First-In-Human Study of PDT to Detect IAH

Not Applicable

Recruiting

• Conditions: Intra-Abdominal Hypertension
• Interventions: Device: Intra-gastrointestinal monitoring device (PDT)

• Registration Number: NCT06333366
• Lead Sponsor: Chang Gung Memorial Hospital

Brief Summary

PDT is a continuous pressure monitoring for Intra-Abdominal hypertension (IAH) designed to be less invasive than pan-endoscopic evaluation, more tolerable than abdominal tapping, and more effective than intravesical pressure measurement for IAH. The PDT device consists of a piezoelectric sensor module with a low power Bluetooth wireless transmitter encased in biocompatible capsule. The device will be swallowed after activation. Following PDT insertion, the patient is fitted with a custom, removable external waist accessory containing a receiver, which is worn during monitoring and provide PDT location by signal analysis with sufficient information to provide IAH trends.

Detailed Description

The participant will receive first phantom capsule after complete survey before the test, which include standard clinical intra-vesical pressure measurement in the perioperative period of laparoscopic surgery. The phantom capsule is an equal-weighted device of the same outer shell but without the electric circuits. After the phantom capsule has been passed out, the participant will receive the standard PDT capsule to record measured information continuously. The date of the laparoscopic surgery should be within follow-up day 2 to day 6. Standard clinical intra-vesical pressure measurement will only be applied in the perioperative period of laparoscopic surgery. The participant will still be monitored by standard PDT capsule afterwards. After the PDT capsule passed out, the participant will receive complete checkup again for comparison.

Study Timeline

• Study Start: 2024-02-18
• Study First Submitted: 2024-02-20
• Status Verified: 2024-03
• Study First Submitted QC: 2024-03-20
• Last Update Submitted: 2024-03-20
• Study First Posted: 2024-03-27
• Last Update Posted: 2024-03-27
• Primary Completion: 2024-07-16
• Study Completion: 2025-09-20

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Patient volunteer planning for laparoscopic surgery
• Subjects willing to sign an informed consent form (ICF),
• Adult subjects, age ≥ 20 and age ≤ 80 years old
• BMI between 15（kg/m2）- 35（kg/m2）
• Subjects willing to comply to study protocol requirements (blood pressure measurement, diet, alcohol, study visits, blood sampling, etc.)
• Patient who had been scheduled for any laparoscopic surgery which may alter intra-abdominal pressure.
• Patient volunteer planning for laparoscopic surgery, as self-declared and confirmed by screening assessments and Principal Investigator's judgment

Exclusion Criteria

• Patients with a high risk for capsule retention (such as intestinal diverticula, acute abdominal pain without regular defecation indicating intestinal obstruction or a history of abdominal operation or intestinal reconstructed operation),
• Any evidence that occlusion of gastrointestinal tract is obvious or severe paralytic ileus that may result in intra-abdominal hypertension in need of immediate surgical intervention not caused by base of tongue (i.e., central apnea, neurologic disorder, retropalatal collapse, nasal obstruction)
• Any condition that subject is expected to undergo MRI examination within 7 days after ingestion of the capsule.
• Any factor that, in the surgeon's judgment, would pose a risk to surgery or placement of an intra-gastrointestinal monitoring device
• Any factor that, in the surgeon's judgment, would make the subject unlikely to respond to PDT insertion and pressure measurement.
• Congenital anomalies of gastrointestinal tract or any other anatomical abnormality of the head, neck, chest, or abdomen that would be a contraindication to placement of the PDT device and usage of the external device
• There are no exclusion criteria based on gender, race or ethnicity
• Patients with a history of Crohn's disease i* Patients with serious systematic diseases such as congestive heart failure, renal failure or severe liver disease.
• Any blood disorder identified by haematocrit <30% or >55%
• History of hepatitis B, hepatitis C, or HIV
• Subject has had prior abdominal surgery of the gastrointestinal tract other than uncomplicated procedures that would be unlikely to lead to bowel obstruction based on the clinical judgment of the investigator
• Female subjects who are pregnant, planning on becoming pregnant or nursing
• Any disorder, which in the investigator's opinion might jeopardise subject's safety or compliance with the protocol.
• Coagulation disorder, wound healing and bleeding disorder or taking anticoagulant medication
• The presence of any other active implanted device, such as cardiac pacemaker or other implanted electro medical devices.
• The presence of any other wireless sensor or transmitter located in abdomen (excluding compatible device also for pressure sensing and other location is acceptable)
• Impaired fasting glucose or impaired glucose tolerance (for Patient volunteer planning for laparoscopic surgery)
• Any contraindication to the use of the PDT system as listed in the device Instructions for Use (IFU) (i.e. any known allergy to PDMS)
• Subject has dysphagia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
intraabdominal pressure (IAP) monitor	Intra-gastrointestinal monitoring device (PDT)	Patient who will take laparoscopic surgery will be checked for intra-abdominal pressure, intra-vesical pressure, and intra-gastrointestinal pressure ri-operative stage. PDT passage time will be checked.

Primary Outcome Measures

Name	Time	Method
Rate of GI symptoms, i.e. inflammation, infection, diarrhea, bowel obstruction, and ileus	15 days	evaluating safety
Incidence of sensor failure	15 days	evaluating stability of device
Incidence of device-related or sensor insertion/removal procedure-related adverse events	15 days	evaluating of incidence of adverse event (AE)
Rate of foreign body reaction due intra-gastrointestinal insertion	15 days	evaluating GI symptoms

Secondary Outcome Measures

Name	Time	Method
Duration of PDT insertion and explantation procedure	15 days	monitoring usability needs
Incidence of side effects in Post explantation follow-up	30 days	follow up for sequel
Rate of GI dysfunction after 10 days post explantation of the PDT sensor. Follow-up via phone call after 30 days	30 days	monitoring of GI symptoms
Percentage of users feedback in the form of clinical questionnaire to assess the 'easiness' of insertion procedure with questionnaire	1 day	evaluating feed back

Trial Locations

Locations (1)

Dong-Ru Ho; 🇨🇳 Chiayi City, Taiwan