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NCT05784493 Clinical Trial

Pain After Laparoscopic Hysterectomy

Postoperative Pain Clinical Trial

Official title:
The Effect of Intraabdominal Saline Washing After Laparoscopic Hysterectomy on Postoperative Pain: Double Blind Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05784493
Other study ID # 2020.04.06.02
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date December 30, 2020

Study information
Verified date March 2023
Source Namik Kemal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators evaluated postoperative pain after total laparoscopic hysterectomy. Two arm are evaluated. During laparoscopic hysterectomy, in one arm; abdominal cavity was washed by saline at normal room temperature. In another arm; abdominal cavity was washed heated saline . Postoperative pain was evaluated by using visual analogy scale.

Description:

The aim of this study was evaluated the effect of washing abdominal cavity by heated or normal temperature saline on postoperative pain. This study is double blind randomized controlled study. inclusion criteria: all of cases that had laparoscopic hysterectomy for bening condition exclusion criteria: maling cases and conversion to laparotomy after randomization and completion of surgery, investigator was evaluated postoperative pain at 0-4-8 th hours by using visual analog scale participants and investigator were blinded .

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date December 30, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - all of cases that had laparoscopic hysterectomy for bening conditions Exclusion Criteria: - maling cases - conversion to laparotomy

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Study group
Washing by heated saline group

Locations
Country Name City State
Turkey Namik Kemal University Tekirdag

Sponsors (4)
Lead Sponsor Collaborator
Namik Kemal University Firat Can Sogut, Mehmet Veysel Arin, Ozlem Sevinc Ergul

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain assessed by visual analog scale To assess postoperative pain incidence by using visual analog scale 5 months
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