Completed
Laparoscopica Hindgut Resection Plus Rectum Suspention Compare With Transanal Rectal Mucosa Resection for ODS With Rectal Prolapse
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Constipation+1
+ Signs and Symptoms
+ Signs and Symptoms, Digestive
From 18 to 80 Years
+4 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: January 2018
Summary
Principal SponsorThird Military Medical University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Study start date: January 8, 2018
Actual date on which the first participant was enrolled.Chronic obstinate constipation is hard to deal with in clinic. Especially for obstructed defecation syndrome(ODS). Rectal prolapse is the most common type of ODS. Lots of surgical procedures have been suggested for it but with unsatisfactory results.To develop new surgical treatment and to provide higher quality proof for this intractable condition is of significance.
Official TitleLaparoscopica Hindgut Resection Plus Rectum Suspention Compare With Transanal Rectal Mucosa Resection for ODS With Rectal Prolapse
Principal SponsorThird Military Medical University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
16 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
ConstipationSigns and SymptomsSigns and Symptoms, DigestivePathological Conditions, Signs and Symptoms
Criteria
2 inclusion criteria required to participate
Diagnosed with ODS by defecography, coloscopy, barium enema and dynamic MRI.
Patients should accord with Rome IV criteria.
2 exclusion criteria prevent from participating
Severe heart or other organ disease.
test.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Suspended
CompletedOne Study Center