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NCT06159777 · ClinicalTrials.gov registry record · Phase 4
Pre-operative Polyethylene Glycol 3350 for Minimally Invasive Urogynecologic Surgery
A Phase 4 study of Constipation and Surgical Procedure, Unspecified, sponsored by University Hospitals Cleveland Medical Center.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 74
- Enrollment target
- 1
- Study location
NCT06159777: Recruiting Phase 4 study of Constipation and Surgical Procedure, Unspecified, sponsored by University Hospitals Cleveland Medical Center.
NCT06159777 is a Phase 4 study of Constipation and Surgical Procedure, Unspecified that is actively recruiting participants, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 74 participants, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (64% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06159777, a Phase 4 study of Constipation and Surgical Procedure, Unspecified, is actively recruiting participants, sponsored by University Hospitals Cleveland Medical Center.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 74 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to test the use of a laxative before surgery in women having surgery to fix pelvic prolapse that do not have constipation. The main question it aims to answer is: Does use of a laxative before surgery lessen the discomfort of bowel movements after surgery? Participants will be asked to complete questionnaires before and after surgery. Researchers will compare using the laxative before and after surgery versus only after surgery to see if there is less discomfort with bowel movements after surgery.
Primary Outcome
Patient assessment of constipation symptoms (PAC-SYM) is a validated 12-item questionnaire with reported average score 0-4.
Conditions Studied
Interventions
- DRUG Polyethylene Glycol 3350
Study Locations (1)
Ohio
- University Hospitals Cleveland Medical Center - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2024-06-05 |
| Est. Completion | 2026-04-30 |
| Phase | Phase 4 |
What NCT06159777 shows while recruiting
NCT06159777 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 204-participant average among 54 other Constipation trials with a reported enrollment target (64% lower).
The record links to 3 conditions, with Constipation appearing as the primary indexed condition, and to 1 intervention - of which Polyethylene Glycol 3350 is the first listed.
NCT06159777 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT06159777 about?
NCT06159777 is a clinical study titled "Pre-operative Polyethylene Glycol 3350 for Minimally Invasive Urogynecologic Surgery". The goal of this clinical trial is to test the use of a laxative before surgery in women having surgery to fix pelvic prolapse that do not have constipation. The main question it aims to answer is: Does use of a laxative before surgery lessen the discomfort of bowel movements after surgery? Partici...
What is the current status of trial NCT06159777?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 74 participants. The study started on 2024-06-05. Estimated completion is 2026-04-30.
What conditions does trial NCT06159777 study?
This clinical trial studies the following conditions: Constipation, Surgical Procedure, Unspecified, Prolapse; Female.
What interventions are being tested in trial NCT06159777?
The interventions under investigation include: Polyethylene Glycol 3350 (DRUG).
Who is sponsoring clinical trial NCT06159777?
This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06159777 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Constipation
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06159777's enrollment target sits among peer trials
74 25th of 54 higher than 30 of 54 other Constipation trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Constipation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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An Open Label Study of Chronic Polyethyleneglycol3350 Use in Constipated Patients
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Comparison of PolyethyleneGlycol and Placebo for Relief of Constipation From Constipating Medications
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-
Preference of Tegaserod vs. PEG 3350 in Patients With Constipation
COMPLETED · Phase 4
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