Quadratus Lumborum Type II Block vs Quadratus Lumborum Type III Block in patients undergoing Total Laparoscopic Hysterectomy

Not yet recruiting

• Conditions: Other Procedures,

• Registration Number: CTRI/2021/02/031408
• Lead Sponsor: Not Funded

Brief Summary

Total LaparoscopicHysterectomy is one of the regularly done laparoscopic surgeries in many partsof the world. The postoperative painfollowing Total Laparoscopic Hysterectomy might be because of pneumoperitoneum,intra-abdominal peritoneal stretching and from operated area in pelvic region,which is mainly visceral type. Thus, single mode of analgesia, most commonly byNSAIDS or Opioids is not enough for the patient to have a smooth postoperativerecovery. The quadratus lumborum block is anew abdominal truncal block used for analgesia of both the upper and lowerabdominal surgeries. Quadratus lumborum block allows the local spread of drugsbetween the posterior aspect of muscle and middle layer of thoracolumbarfascia. The Hypothesis of this study is that Quadratus Lumborum Type III block will provide better perioperative analgesia and decrease the total analgesic consumption in postoperative period.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2021-02-18
• Study Start: 2021-02-22

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

• 1. All patients aged between 30-60 years.
• 2. ASA I & II 3) Patients undergoing Total Laparoscopic Hysterectomy.

Exclusion Criteria

1. Patient Refusal 2) Patients with underlying severe cardiopulmonary compromise 3) Total Laparoscopic Hysterectomy converted to Total Abdominal Hysterectomy 4) Morbid Obesity BMI more than or equal to 35 5) Allergy to Local Anaesthetics 6) Patients already on prescribed psychotropic agents 7) Coagulation Disorders.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the total amount of analgesic consumption in 24 hours	To compare the total amount of analgesic consumption in 24 hours

Secondary Outcome Measures

Name	Time	Method
To compare the time to first rescue analgesia	To compare the mean Numerical Rating Score (NRS) of pain, in first 24 hours (measured at 1, 6, 12 and 24 hrs.)

Trial Locations

Locations (1)

AIIMS PATNA; 🇮🇳 Patna, BIHAR, India

AIIMS PATNA

🇮🇳Patna, BIHAR, India

DR RAJNISH KUMAR

Principal investigator

7783865337

drraj76pmch@gmail.com