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Surgical outcomes using bowel enema before benign gynecologic laparoscopic surgeries

Surgical and Patient Outcomes Using Normal Saline Enema for Bowel Preparation Before Benign Gynecologic Laparoscopic Surgeries

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110530006640N6
Enrollment
112
Registered
2020-07-21
Start date
2020-07-20
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign gynecology disease. Other noninflammatory disorders of uterus, except cervix

Interventions

Intervention 1: Intervention group:Patients eat light meals and fluids the night before surgery and they become NPO from 12 midnight . Intervention for this group is enema with normal saline once at 1

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients who are candidates for level 2 and 3 laparoscopic gynecologic surgeries

Exclusion criteria

Exclusion criteria: Patients who are at risk for intestinal injury during laparoscopy and are candidates for complete bowel preparation before surgery such as : a history of multiple previous surgery with many adhesion, sever endometriosis in cul de sac and bowel/large uterus with adhesion in hysterectomy,cancer surgery, surgery in sever PTD with abcess. Patients who are candidates for level 1 laparoscopic surgeries such as TL and diagnostic laparoscopy. Patients who are candidates for level 4 laparoscopy surgeries such as lymphadenectomy,sever endometriosis, presacral neurectomy History of patients intestinal diseases such as IBS and colitis Severe obesity (BMI>35)

Design outcomes

Primary

MeasureTime frame
Surgeon's satisfaction from intraoperative visualization and bowel handling. Timepoint: Immediately after surgery. Method of measurement: Questionnaire.;Complication of surgery such as viscoralinjury , fever, decrease of hemoglobin. Timepoint: Intraoperative and after surgery. Method of measurement: Patient File.

Secondary

MeasureTime frame
Duration of surgery. Timepoint: End of surgery. Method of measurement: Cornometer.;Duration of hospitalization. Timepoint: Time of the discharge from the hospital. Method of measurement: Day/Patient file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Zahra Asgari

Tehran University of Medical Sciences

asgariza@sina.tums.ac.ir+98 21 7788 8755

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026