Patients Response in Laparoscopic Gynaecological Surgeries Following Instillation Of Levo-Bupivacaine Intraperitoneally

Not Applicable

Completed

• Conditions: Health Condition 1: D279- Benign neoplasm of unspecified ovaryHealth Condition 2: N809- Endometriosis, unspecifiedHealth Condition 3: D251- Intramural leiomyoma of uterusHealth Condition 4: N925- Other specified irregular menstruation

• Registration Number: CTRI/2019/07/020152
• Lead Sponsor: DR ASIF MUSTAFA

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-06-12
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 90

Inclusion Criteria

The study will include ASA-I &II women presenting to Max Smart super specialty Hospital Saket for elective laparoscopic Gynecological surgery meeting the inclusion criteria as described below:

1) ASA I &II patients.

2) Age 18-70yrs.

3) elective surgery

Exclusion Criteria

The study will include ASA-I &II women presenting to Max Smart super specialty Hospital Saket for elective laparoscopic Gynecological surgery with exclusion criteria as described below:

1) ASA III and above patients

2) Use of opioids within 24hrs prior to study

3) Drugs & alcohol abuse

3) History of allergy to any drug used in study.

4) Patients having chronic pain syndrome

5) Treatment with steroids prior to surgery

6) Patient with diagnostic laparoscopy without surgical procedure.

7) Patients who do not understand VAS pain scale.

8) Patients not willing to be included in the study- not giving consent.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate whether instillation of levo-bupivacaine intraperitoneal decreases post operative pain after laparoscopic gynecological surgeries, using VAS pain Scale.Timepoint: 24 HOURS POST SURGERY

Secondary Outcome Measures

Name	Time	Method
1.To assess requirement of rescue analgesia in post operative periods.Timepoint: Hourly till 24 Hours Post Surgery;2.To assess whether the incidence of PONV (post operative nausea and vomiting) reduces in the study group. <br/ ><br>Timepoint: 24 HOURS POST SURGERY