Transanal Irrigation for the Management of Early Low Anterior Resection Syndrome (LARS): A Pilot Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Patient-Reported Outcomes Measurement Information System (PROMIS)-GI Diarrhea at baseline
研究概览
简要总结
Transanal irrigation (TAI) has shown to improve fecal incontinence and increase quality of life in patients with low anterior resection syndrome (LARS). This trial is a small study being conducted to determine whether a larger trial is feasible. Investigators are also doing this research to see if TAI impacts quality of life and improves bowel function within the early post-operative period (1-12 months).
This treatment is designed for participants to have more control over their bowel movements and reduce the dependency on immediate access to the toilet.
详细描述
Colorectal cancer is the third most common cancer in the U.S. with 152,810 new cases estimated for 2024. Rectal cancer comprises one-third of all incident cases, with rising incidence among young individuals (1-2% rise/year). With advances in multidisciplinary management, the overall, 5-year survival has improved (68%), and for localized rectal cancers it is excellent (90%), creating a growing rectal cancer survivorship population (currently >450,000). Traditionally, surgery for rectal cancer required removal of the rectum and the anus, with the creation of a permanent ostomy. However, with recent advances in subspecialty training and technique, in combination with neoadjuvant radiation, surgeons can offer a cure while preserving the anal sphincter and restoring bowel continuity, via a newer technique called Low Anterior Resection (LAR). This technique, favored by surgeons and patients, aims to allow patients to have an option of remaining "close to normal", as opposed to having a permanent ostomy. While this technique has been successful in sparing the rectum, these advancements have not come without consequence. Bowel dysfunction post-LAR, known as Low Anterior Resection Syndrome (LARS), is perhaps the most prevalent and significant sequela, affecting up to 70-90% of rectal cancer survivors. LARS symptoms include fecal incontinence, urgency, increased frequency, stool fragmentation, and incomplete evacuation. These uncontrolled LARS symptoms have a devastating impact on patients' quality of life (QoL), and often persist indefinitely. Treatment for LARS focuses on symptom management, using diet, medications and pelvic floor physiotherapy, but these measures often fail leaving patients with significant symptoms. Consequently, many patients are unable to return to work in their prior roles and require long-term disability or early retirement. Patients also resort to lifestyle restrictions including skipping meals, restricting social and recreational activities, and avoiding travel and exercise, thereby further diminishing their QoL .
Transanal irrigation (TAI) is an established treatment used for fecal incontinence and constipation. TAI is designed to irrigate a large amount of water throughout the entire colon, allowing for scheduled and complete emptying of stool. As such, TAI has the potential to reduce the symptoms of LARS including difficulty emptying, incontinence, and frequent, unpredictable bowel movements. This single daily irrigation is designed to allow patients to be free of bowel movements during the day and reduce their dependency on immediate access to the toilet, thus decreasing the impact of LARS on their daily lives. Currently, TAI is not in wide clinical use for LARS in North America despite reports from small prospective European studies (15-37 patients) demonstrating benefits for LARS . The most recent and robust published study to date, included patients with late LARS (>1-year post-treatment) randomized to TAI (n=16) vs. control (n=22), and reported significant improvements in LARS and QoL at 1 year when using TAI.
Prior work: Investigators have conducted a multi-center, cross-over, pragmatic randomized controlled trial (RCT) to assess TAI for late LARS (median 2 years post-treatment) at 7 Canadian institutions (NCT04469426). The trial has completed accrual (n=71). Patients were randomized (1:1 ratio) to start in either the TAI or control group, and then crossed over to the opposite group. Participants spent 3 months in each arm. Participants in the TAI arm received nursing instruction and online education for learning TAI using the "LARS-TAI" app. I created this web-based HIPAA-compliant, mobile app (iOS™ and Android™ compatible) to support patients with LARS using TAI. The LARS-TAI App is accessible on any device with internet access or cellular data, including smart phones, tablets, and computers. The app contains educational modules on LARS and TAI, a discussion forum, patient videos, and bowel diaries. Investigators are currently completing follow-up and data analysis for this study. This cross-over trial has provided invaluable practical knowledge on educating patients about TAI and has demonstrated a high level of acceptance for TAI as a treatment for LARS within the first North American sample. Furthermore, it has underscored the challenges associated with a cross-over study design, as many participants were hesitant to transition from TAI to the control group due to the marked improvements in LARS and QoL that they experienced with the intervention.
At CCF-FL, I have established a LARS Clinic, with a trained LARS nurse, and investigators have treated over 50 rectal cancer patients with LARS in 2024. Investigators have established a LARS registry and are routinely screening for LARS in our rectal cancer patients. Investigators have partnered with CCF-Ohio who have also started screening rectal cancer patients for LARS. Investigators have identified a high burden (75% major LARS) of LARS post-treatment in our rectal cancer patients.
The knowledge gap: While TAI shows promise for LARS management, the optimal timing for its use remains unclear. The first 6 months post-treatment pose significant challenges for LARS patients, with at least 58% experiencing major LARS and significantly decreased quality of life (QoL). Investigators observed that 54% of these patients with major LARS also experience financial distress, with most unable to return to work. Unfortunately, conservative measures often fail in this early phase, rendering patients in despair as they try to adapt to their altered bowel function. The potential for TAI to improve LARS in this early phase was proposed in a small German RCT (n=37) that demonstrated reduced bowel movements and improved LARS with no significant complications .
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults (≥18 years-old) patients who underwent a LAR for any indication via open, laparoscopic, robotic, or transanal total mesorectal excision, with creation of a diverting loop ileostomy,
- •have confirmed anastomotic healing demonstrated by flexible sigmoidoscopy and CT scan with rectally-administered water soluble contrast or gastrograffin enema,
- •are planned for an ileostomy closure operation, and
- •are in the first 12 months post-LAR operation
排除标准
- •Inability to comprehend English or Spanish or provide informed consent (Note: after the English documents are approved, the study team plans to obtain a Spanish consent and study documents),
- •ongoing chemotherapy or radiotherapy, and
- •ongoing anastomotic complication.
研究组 & 干预措施
Transanal Irrigation (TAI) - intervention arm
Participants in the TAI-intervention arm will receive TAI (using Peristeen Plus Irrigation kit), training of TAI administration, and access to the LARS app (including TAI module).
干预措施: Peristeen Plus Irrigation kit (Device)
Transanal Irrigation (TAI) - intervention arm
Participants in the TAI-intervention arm will receive TAI (using Peristeen Plus Irrigation kit), training of TAI administration, and access to the LARS app (including TAI module).
干预措施: LARS mobile application (Other)
Continued conservative management - control arm.
Participants in the control arm will receive conservative management and access to the LARS app (excluding the TAI module). Conservative management includes individualized combinations of dietary modifications, pharmacologic therapies, pelvic floor rehabilitation, and structured follow-up
干预措施: LARS mobile application (Other)
结局指标
主要结局
Patient-Reported Outcomes Measurement Information System (PROMIS)-GI Diarrhea at baseline
时间窗: Baseline
PROMIS\_GI Diarrhea with domains covering Frequency, urgency, burden. T-score (mean = 50, SD = 10); higher scores = worse diarrhea
Patient-Reported Outcomes Measurement Information System (PROMIS)-GI Diarrhea at 1 month
时间窗: 1 month post randomization
PROMIS\_GI Diarrhea with domains covering Frequency, urgency, burden. T-score (mean = 50, SD = 10); higher scores = worse diarrhea
Patient-Reported Outcomes Measurement Information System (PROMIS)-GI Diarrhea at 2 months
时间窗: 2 months post randomization
PROMIS\_GI Diarrhea with domains covering Frequency, urgency, burden. T-score (mean = 50, SD = 10); higher scores = worse diarrhea
Patient-Reported Outcomes Measurement Information System (PROMIS)-GI Diarrhea at 3 months
时间窗: 3 months post randomization
PROMIS\_GI Diarrhea with domains covering Frequency, urgency, burden. T-score (mean = 50, SD = 10); higher scores = worse diarrhea
PROMIS-GI Fecal Incontinence at baseline
时间窗: Baseline
PROMIS\_GI Fecal Incontinence with domains covering Leakage, control, impact . T-score (mean = 50, SD = 10); higher scores = worse incontinence
PROMIS-GI Fecal Incontinence at 1 month
时间窗: 1 month post randomization
PROMIS\_GI Fecal Incontinence with domains covering Leakage, control, impact . T-score (mean = 50, SD = 10); higher scores = worse incontinence
PROMIS-GI Fecal Incontinence at 2 months
时间窗: 2 months post randomization
PROMIS\_GI Fecal Incontinence with domains covering Leakage, control, impact . T-score (mean = 50, SD = 10); higher scores = worse incontinence
PROMIS-GI Fecal Incontinence at 3 months
时间窗: 3 months post randomization
PROMIS\_GI Fecal Incontinence with domains covering Leakage, control, impact . T-score (mean = 50, SD = 10); higher scores = worse incontinence
Average monthly randomization rate
时间窗: 3 months post ileostomy
Participants who report a LARS Score of ≥20-the threshold for moderate-to-severe LARS-will meet criteria for randomization. Score range: 0-42 (higher scores = more severe LARS; 0-20 = no LARS, 21-29 = minor, 30-42 = major)
次要结局
- PROMIS Physical Function at baseline(Baseline)
- PROMIS Physical Function at 1 month(1 month post randomization)
- PROMIS Physical Function at 2 months(2 months post randomization)
- PROMIS Physical Function at 3 months(3 months post randomization)
- PROMIS Ability to Participate in Social Roles and Activities at baseline(Baseline)
- PROMIS Ability to Participate in Social Roles and Activities at 1 month(1 month post randomization)
- PROMIS Ability to Participate in Social Roles and Activities at 2 months(2 months post randomization)
- PROMIS Ability to Participate in Social Roles and Activities at 3 months(3 months post randomization)
- PROMIS Anxiety at baseline(Baseline)
- PROMIS Anxiety at 1 month(1 month post randomization)
- PROMIS Anxiety at 3 months(3 months post randomization)
- PROMIS Depression at baseline(Baseline)
- PROMIS Depression at 1 month(1 month post randomization)
- PROMIS Anxiety at 2 months(2 months post randomization)
- PROMIS Depression at 2 months(2 months post randomization)
- PROMIS Depression at 3 months(3 months post randomization)
- PROMIS Sleep Disturbance at baseline(Baseline)
- PROMIS Sleep Disturbance at 1 month(1 month post randomization)
- PROMIS Sleep Disturbance at 2 months(2 months post randomization)
- PROMIS Sleep Disturbance at 3 months(3 months post randomization)
- PROMIS Satisfaction with Social Roles at baseline(Baseline)
- PROMIS Satisfaction with Social Roles at 1 month(1 month post randomization)
- PROMIS Satisfaction with Social Roles at 2 months(2 months post randomization)
- PROMIS Satisfaction with Social Roles at 3 months(3 months post randomization)
- PROMIS Self-Efficacy for Managing Chronic Conditions at baseline(Baseline)
- PROMIS Self-Efficacy for Managing Chronic Conditions at 1 month(1 month post randomization)
- PROMIS Self-Efficacy for Managing Chronic Conditions at 2 months(2 months post randomization)
- PROMIS Self-Efficacy for Managing Chronic Conditions at 3 months(3 months post randomization)
- Completeness(3 months post randomization)
- Treatment adherence rate(3 months post randomization)
- Consent rates(Post consenting, Baseline)
