Better pain relief after Laparoscopic hysterectomy surgery using numbing shot and paracetamol together .

Phase 2

• Conditions: Health Condition 1: N920- Excessive and frequent menstruation with regular cycle

• Registration Number: CTRI/2024/04/065917
• Lead Sponsor: Sri Manakula Vinayagar Medical College and Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.Age between 18 and 65 years

2.American Society of Anesthesiologists physical status (ASAPS) classification I-II

3.Planned for laparoscopic hysterectomy (includes total laparoscopic hysterectomy, laparoscopic supracervical hysterectomy, laparoscopically assisted vaginal hysterectomy, with or without salpingo-oophorectomy)

Exclusion Criteria

1.History of cervical surgery such as conization or cerclage.

2.Inability to perform the para-cervical block due to anatomical abnormalities (i.e., very atrophicor small cervix).

3.Allergy to bupivacaine, planned concomitant surgical procedures involving extensive

additional tissue manipulation such as pelvic lymph node dissection.

4.Previously taking opioids for chronic pain.

5.Chronic PID, endometriosis

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess the efficacy of preoperative para-cervical block with 0.25% bupivacaine as an adjuvant with intravenous paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy.Timepoint: At 30minutes,60minutes,2hours,4hours,6hours,8hours.

Secondary Outcome Measures

Name	Time	Method
To assess the efficacy of perioperative paracervical block with bupivicaine as an adjuvant with paracetamol on postoperative pain relief in patients undergoing laparoscopic hysterectomy.Timepoint: at 30minutes,60minutes,2hours,4hours,6hours,8hours.