CClinicalTrials.gg
RecruitingNCT07605533Updated May 26, 2026

Accuracy of Transabdominal Ultrasound in Predicting Intraperitoneal Adhesions Prior to Laparoscopy

An observational study in Intraperitoneal Adhesions, sponsored by Sohag University. Recruiting at 1 site in Egypt. Open to female participants. Per ClinicalTrials.gov, last updated 2026-05-26.

Sponsored by Sohag University · Observational

From the registry’s dates

  • Started May 2025; still recruiting 1 year 5 months later.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
74
Sex
Female
01

Study summary

Detecting Accuracy of transabdominal ultrasound in detecting intraperitoneal adhesions prior to laparoscopy ( which is the gold standard to visualize adhesions ) to detect safety of 1ry trocar insertion .

02

Conditions studied

  • Intraperitoneal Adhesions

Keywords

  • intraperitoneal adhesions
03

In context

Lead sponsor

Sohag University is the lead sponsor of 1,183 studies on the registry; 612 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Women undergoing laparoscopic surgery in the department of gynecology \& obstetrics , Sohag University hospital with the following criteria :

Women scheduled for elective laparoscopy. Women with history of previous laparotomies. Women with previous transverse suprapubic and/or any midline incision. Women with previous caesarean section.

Inclusion criteria

  • Women scheduled for elective laparoscopy.
  • Women with history of previous laparotomies.
  • Women with previous transverse suprapubic and/or any midline incision.
  • Women with previous caesarean section.

Exclusion criteria

Exclusion Criteria:

  • Women with Emergency laparoscopic surgeries (e.g., acute abdomen).
  • Pregnancy at time of operation.
  • Morbid obesity (BMI > 40kg/m²), as excessive adipose tissue may limit ultrasound imaging.
  • Severe medical conditions affecting participation (e.g., severe cardiac or pulmonary disease.
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
74 participants (estimated)
Patient registry
No

Groups and cohorts

  • patients with previous abdominal surgery undergoing laparoscopic Surgery

    Procedure: laparoscopy · Diagnostic Test: transabdominal ultrasound

Interventions

  • Procedurelaparoscopy

    Laparoscopy

  • Diagnostic testtransabdominal ultrasound

    Transabdominal ultrasound sliding sign

06

What researchers measure

Primary outcomes

  1. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of Transabdominal sliding sign for detection of intraperitoneal adhesions

    Time frame: Day 1 (from patient selection until the laparoscopic operation is done and presence and type of adhesions is revealed.)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07605533
Lead sponsor
Sohag University
Responsible party
Mohamed Shabaan Abohamady (Accuracy of Transabdominal Ultrasound in Predicting Intraperitoneal Adhesions Prior to Laparoscopy, Sohag University) — Principal investigator
First posted
May 26, 2026
Start date
May 1, 2025
Primary completion
Aug 1, 2026 (estimated)
Completion
Aug 1, 2026 (estimated)
Last update
May 26, 2026

Study contacts

Mohamed Abu Hammady, Resident
Contact
shabanhegazy@gmail.com
00201142217180 ext. 00201080768575

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion