Efficacy of Laparoscopic AdhesiolysisNCT06799208
Laparoscopic Approach in Adhesive Intestinal Obstruction
An observational study of Efficacy of Laparoscopic Adhesiolysis, run by Assiut University.
Trial summary
A Clinical trail to evaluate the efficacy of Laparoscopic approach in Adhesive Intestinal Obstruction . Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Efficacy of Laparoscopic Adhesiolysis
- What is being tested?
- Laparoscopy
- Type of treatment
- Surgery or procedure
- How many people
- 40 participants
- Where
- No sites listed yet
- Study dates
- Mar 2026to May 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: All patients admitted to General Surgery department with adhesive intestinal obstruction during the year of study.
Who may be able to join
- Patient who clinically diagnosed as adhesive intestinal obstruction.
- Both sexes
- Adult patients (above 18 years old
Who cannot join
- • Patient refused to participate in this study.
- Patients not fit for laparoscopic surgery.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
Mohammad Sayed Mohammad Sayed Mohammad Ibrahim, General Surgery Resident contact
About this study
Official title: Evaluating the Efficacy of Laparoscopic Approach in Adhesive Intestinal Obstruction
A Clinical trail to evaluate the efficacy of Laparoscopic approach in Adhesive Intestinal Obstruction .
Read the detailed description
There was a rapid growth of minimally invasive operations. Through its peritoneal tissue sparing character and minimal blood loss, laparoscopy was soon claimed to reduce adhesion formation and associated complications.
The aim of this prospective clinical trial study is to evaluate the use of laparoscopy in management of clinically diagnosed adhesive intestinal obstruction and the criteria of selection to get the best results .
- Conditions
- Efficacy of Laparoscopic Adhesiolysis
- Being tested
- Laparoscopy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
LaparoscopyProcedure or surgery
Minimal invasive approach. Have peritoneal tissue sparing character . Minimal blood loss . Reduction of postoperative adhesions.
| Study group | Role | What they receive |
|---|---|---|
| Patient diagnosed with intestinal obstruction | Not described Receives: Procedure: Laparoscopy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of days post- operative till passing stool .
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Jan 2025
- Study startMar 2026 (estimated)
- Primary completionMar 2027 (estimated)
- Study completionMay 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Efficacy of Laparoscopic AdhesiolysisStudies of the same condition, open and under way.
- More trials run by Assiut UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assiut University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mohammad Sayed Mohammad Ibrahim, Assiut University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06799208
- Sponsor's protocol ID
- Laparoscopic adhesiolysis
- Status last verified
- Jan 2025
- First submitted
- 10 Jan 2025
- Last updated
- 29 Jan 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluating the Efficacy of Laparoscopic Approach in Adhesive Intestinal Obstruction
- ClinicalTrials.gov ID
- NCT06799208
- Acronym / sponsor ID
- Laparoscopic adhesiolysis
- Conditions
- Efficacy of Laparoscopic Adhesiolysis
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Assiut UniversityUniversity, hospital or other
- Study start
- Mar 2026 (estimated)
- Primary completion
- Mar 2027 (estimated)
- Study completion
- May 2027 (estimated)
- First posted
- 29 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A Clinical trail to evaluate the efficacy of Laparoscopic approach in Adhesive Intestinal Obstruction .
Detailed description
There was a rapid growth of minimally invasive operations. Through its peritoneal tissue sparing character and minimal blood loss, laparoscopy was soon claimed to reduce adhesion formation and associated complications.
The aim of this prospective clinical trial study is to evaluate the use of laparoscopy in management of clinically diagnosed adhesive intestinal obstruction and the criteria of selection to get the best results .
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patient diagnosed with intestinal obstruction | – | Procedure: Laparoscopy |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All patients admitted to General Surgery department with adhesive intestinal obstruction during the year of study.
Key inclusion criteria (3 listed)
- Patient who clinically diagnosed as adhesive intestinal obstruction.
- Both sexes
- Adult patients (above 18 years old
Key exclusion criteria (2 listed)
- • Patient refused to participate in this study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LaparoscopyMinimal invasive approach. Have peritoneal tissue sparing character . Minimal blood loss . Reduction of postoperative adhesions. | Procedure or surgery | Patient diagnosed with intestinal obstruction |
Primary outcome
Number of days post- operative till passing stool .
Time frame: 1 year
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Jan 2025.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Mohammad Sayed Mohammad Sayed Mohammad Ibrahim, General Surgery Resident contact
Questions about this trial
What is this clinical trial studying?
An observational study of Efficacy of Laparoscopic Adhesiolysis, run by Assiut University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 29 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mohammad Sayed Mohammad Sayed Mohammad Ibrahim, General Surgery Resident (02+01123368767, abdeldayem3151998@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of days post- operative till passing stool . (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Jan 2025.