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The effectiveness of intraperitoneal normal saline infusion and the pulmonary recruitment maneuver to reduce postlaparoscopic shoulder and upper abdominal pain in elective gynecologic surgeries

The effectiveness of intraperitoneal normal saline infusion and the pulmonary recruitment maneuver to reduce postlaparoscopic shoulder and upper abdominal pain in elective gynecologic surgeries

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201402022576N8
Enrollment
280
Registered
2014-05-05
Start date
2014-04-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Laparoscopy. Postprocedural disorders of genitourinary system, not elsewhere classified

Interventions

Intervention 1: Intervention1: pulmonary recruittment manuver,deep respiration by anesthesiologist is done at the end of surgery. Intervention 2: Intervention2:intraperitoneal normal salin ,150ml in
Prevention
Intervention1: pulmonary recruittment manuver,deep respiration by anesthesiologist is done at the end of surgery
Intervention2:intraperitoneal normal salin ,150ml in upper abdomen is left
Intervention3:Pulmonary recruitment manuver+intraperitoneal salin

Sponsors

Research deputy of Tehran university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: The patients selected for screening were all required laparoscopic surgery during the study period. The inclusion criteria were female gender, age 20–65 years old; an American Society of Anesthesiologists physical status classification of I or II, and a willing to undergo laparoscopic surgeries for benign gynecologic lesions, including laparoscopically assisted vaginal hysterectomy, myomectomy, and cystectomy. Patients were excluded from randomization if their disease was malignant, or if they were unwilling to participate.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post operative pain. Timepoint: 2, 4, 6, 12, 24 hours after surgery. Method of measurement: VAS analouge.

Secondary

MeasureTime frame
Nausea. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.;Vomiting. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.;Abdominal distention. Timepoint: 24 hours after surgery. Method of measurement: Questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Davari Tanha

Tehran University of Medical Sciences

fatedavari@yahoo.com+98 21 8889 7764

Outcome results

None listed

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