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A Study of Danning Tablet in Patients With Polypoid Lesions of Gallbladder

Phase 4
Not yet recruiting
Conditions
Polyps Gallbladder
Interventions
Drug: Danning Tablet
Registration Number
NCT05668871
Lead Sponsor
Eastern Hepatobiliary Surgery Hospital
Brief Summary

The primary goal of this clinical trial is to evaluate the effect of Danning Tablet on shrinkage of gallbladder polyps compared to lifestyle intervention in 336 patients with gallbladder polyps. The main questions it aims to answer are:

* Medicine may be effective on shrinkage of gallbladder polyps and alleviation of clinical symptoms of gallbladder polyps.

* Chinese patent medicine (herbal medicine) may be safety in treatment of gallbladder polyps.

Detailed Description

Study design:

In this study, 336 participants will be randomly allocated to the test group or the controlled group in ratio of 1:1 and receive lifestyle intervention from baseline to weeks 24±1. However, in experimental group, participants will take Danning Tablet from baseline to weeks 12±1 (3 times each day, 5 tablets each time). In controlled group, only lifestyle intervention will be adopted. The length of follow-up cycle is 24 weeks.

Evaluation indicators:

Primary indicator: Changes in maximum diameter of gallbladder polyps, use gallbladder ultrasonography to evaluate this indicator on weeks 12±1 and weeks 24±1.

Secondly Indicators:

1. Changes in thickness of gallbladder wall, use gallbladder ultrasonography to evaluate this indicator on weeks 12±1 and weeks 24±1.

2. Changes in clinical symptoms of gallbladder polyps, use Visual Analogue Scale (VAS) to evaluate this indicator on weeks 12±1 and weeks 24±1.

3. Clinical safety indexes, use laboratory examination such as blood biochemical examination, routine blood test for safety observation on weeks 12±1 and weeks 24±1. Besides, observe and record the occurrence of adverse events (AE) of subjects from baseline to follow-up cycle finished.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
336
Inclusion Criteria

Participants suitable for enrollment in this study must meet all of the following criteria:

  1. Be between 18 and 75 years of age, male or female.
  2. More than or equal to 2 gallbladder polyps were detected by B-ultrasound within 2 weeks before enrollment, and the maximum diameter of gallbladder polyps is between 3-7 mm.
  3. No symptoms, or only some non-specific symptoms, such as ventosity, nausea, anorexia, right upper abdominal pain and right shoulder pain, etc.
  4. Provide written informed consent.
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Exclusion Criteria

Participants who meet any of the following criteria will not be eligible for inclusion in this study:

  1. Thickness of gallbladder wall is larger than 6 mm.
  2. Clinically diagnosed as gallbladder cancer.
  3. Clinically diagnosed as gallbladder and/or bile duct stones, and/or acute cholecystitis.
  4. Previously performed gallbladder/biliary tract related operations, such as gallbladder-protected lithotomy, ERCP lithotomy, PTCS lithotomy and PTGBD.
  5. Have severe infectious or severe primary diseases such as diseases in cardiovascular, cerebrovascular, pulmonary, renal or endocrine or hematopoietic system, or with mental diseases and/or behavioral abnormalities, which cannot be enrolled in the study determined by investigator.
  6. Have irregular stool, and/or daily stool frequency more than or equal to 5 times in recent 2 weeks.
  7. Regularly taken any Chinese patent medicine (including traditional Chinese medicine injection) with "soothing liver, cholagogic, clearing heat, dredging intestines" clearly written in the instructions, or regularly taken the traditional Chinese medicine decoction with the effect of soothing liver and cholagogic in recent 4 weeks.
  8. Regularly taken proton pump inhibitors or H2 receptor antagonists or cholinergic receptor antagonists or gastrin receptor antagonists in recent 4 weeks.
  9. Allergic to Danning Tablet and its components, has history of allergy, or has allergic constitution, or in allergic state.
  10. Are pregnant, planning to be pregnant or breastfeeding.
  11. Poor compliance, unable to cooperate with the investigator;
  12. Have previously been involved in another clinical trial in the past three month;
  13. Other situations not suitable for inclusion.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Danning Tablet and lifestyle intervention groupDanning TabletUnder lifestyle intervention, Danning Tablet will be taken orally from baseline to weeks 12±1.
Primary Outcome Measures
NameTimeMethod
Maximum diameter of gallbladder polyps on weeks 12±1weeks 12±1

Use gallbladder ultrasonography to evaluate the maximum diameter of gallbladder polyps.

Maximum diameter of gallbladder polyps on weeks 24±1weeks 24±1

Use gallbladder ultrasonography to evaluate the maximum diameter of gallbladder polyps.

Secondary Outcome Measures
NameTimeMethod
Thickness of gallbladder wall on weeks 24±1weeks 24±1

Use gallbladder ultrasonography to evaluate thickness of gallbladder wall.

Level of abdominal pain on weeks 12±1weeks 12±1

Use Visual Analogue Scale (VAS) to evaluate the level of abdominal pain caused by gallbladder polyps.

Level of abdominal pain on weeks 24±1weeks 24±1

Use Visual Analogue Scale (VAS) to evaluate the level of abdominal pain caused by gallbladder polyps.

Level of abdominal pain on weeks 4±1weeks 4±1

Use Visual Analogue Scale (VAS) to evaluate the level of abdominal pain caused by gallbladder polyps.

Thickness of gallbladder wall on weeks 12±1weeks 12±1

Use gallbladder ultrasonography to evaluate thickness of gallbladder wall.

Level of abdominal pain on weeks 8±1weeks 8±1

Use Visual Analogue Scale (VAS) to evaluate the level of abdominal pain caused by gallbladder polyps.

Clinical safety indexesup to weeks 24±1

Observe and record the occurrence of adverse events (AE) of subjects from baseline to follow-up cycle finished.

Trial Locations

Locations (18)

The First Affiliated Hospital of University of South China

🇨🇳

Hengyang, Hunan, China

Eastern Hepatobiliary Surgery Hospital, Naval Medical University,

🇨🇳

Shanghai, Shanghai, China

Loudi Central Hospital

🇨🇳

Loudi, Hunan, China

Shangrao People's Hospital

🇨🇳

Shangrao, Jiangxi, China

Shanxi Provincial People's Hospital

🇨🇳

Taiyuan, Shanxi, China

The Sixth People's Hospital of Chengdu

🇨🇳

Chengdu, Sichuan, China

Anning First People's Hospital

🇨🇳

Anning, Yunan, China

Affiliated Hospital of Shaoxing University

🇨🇳

Shaoxing, Zhejiang, China

The Second Affiliated Hospital of Zhengzhou University

🇨🇳

Zhengzhou, Henan, China

Affiliated Hospital of Nantong University

🇨🇳

Nantong, Jiangsu, China

First Affiliated Hospital of Gannan Medical University

🇨🇳

Ganzhou, Jiangxi, China

Yiyang Central Hospital

🇨🇳

Yiyang, Hunan, China

Shandong Provincial Third Hospital

🇨🇳

Jinan, Shandong, China

The Affiliated Hospital of Qingdao University

🇨🇳

Qingdao, Shandong, China

Xiangya Changde Hospital

🇨🇳

Changde, Hunan, China

Central Hospital Affiliated to Shandong First Medical University (Jinan Central Hospital)

🇨🇳

Jinan, Shandong, China

Ningbo Municipal Hospital of Traditional Chinese Medicine

🇨🇳

Ningbo, Zhejiang, China

Jinhua Municipal Central Hospital

🇨🇳

Jinhua, Zhejiang, China

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