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studying the effect of nerve block (retrolaminar block) on both sides on reduction in pain intensity in patient operated for laparoscopic guided uterus removal surgery

Ultrasound guided bilateral retro laminar block for post operative analgesia in patients undergoing total laproscopic hysterectomy: A randomised controlled trial - Nil

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098901
Enrollment
100
Registered
2025-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: 1- Obstetrics

Interventions

Intervention1: Ultrasound guided bilateral retro laminar block: The block will be given 30 minutes before the start of surgery and the patient will be followed for 24 hours in the postoperative period

Sponsors

AIIMS, New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA PS I-II, scheduled for total laparoscopic hysterectomy under general anaesthesia.

Exclusion criteria

Exclusion criteria: Patient refusal, allergy to local anaesthetic, cardiac/hepatic/renal dysfunction, BMI more than 30 kg per meter square, infection at site of block, coagulopathy, chronic opioid use, altered mental status.

Design outcomes

Primary

MeasureTime frame
To compare the post operative pain score using numerical rating scale ( NRS ) following ultrasound guided bilateral retro laminar block in patients undergoing total laparoscopic hysterectomy ( 0 = no pain , 10 = worst pain imaginable)Timepoint: 1 hour, 2 hours, 4 hours, 8 hours, 12 hours and 24 hours postoperatively

Secondary

MeasureTime frame
Time to first rescue analgesia.Timepoint: Whenever NRS score is greater than 4, postoperatively for the first 24 hours.;Total intra operative opioid requirement.Timepoint: During the surgery, if heart rate and mean arterial pressure increases more than 20% of baseline values.;Total requirement of rescue analgesia.Timepoint: First 24 hours postoperatively.;To compare post operative recovery using Quality of Recovery-15 ( QoR-15) questionnaire.Timepoint: At first post operative day after 24 hours of anesthesia.;Time to ambulation.Timepoint: 0 to 48 hours.;Complications or side effectsTimepoint: 0 to 48 hours

Countries

India

Contacts

Public ContactDr Nitin Choudhary

AIIMS, New Delhi

drnitinchoudhary@yahoo.in8447698566

Outcome results

None listed

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