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Clinical Trials/NCT03516786
NCT03516786
Completed
Not Applicable

Quality of Recovery After Quadratus Lumborum Block for Cesarean Section: A Prospective Pilot Study

Corniche Hospital1 site in 1 country25 target enrollmentApril 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Corniche Hospital
Enrollment
25
Locations
1
Primary Endpoint
change from baseline postoperative quality of recovery score
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this prospective study is to evaluate the recovery after cesarean section in patients who will receive Quadratus Lumborum Block (QLB) as a part of multimodal analgesia using Postoperative quality of recovery scale.

Detailed Description

Several researchers had evaluated the effectiveness of QLB in controlling postoperative pain in different patient populations. In these studies, the effectiveness of the QLB was mainly assessed by postoperative pain scores and analgesia consumption, rather than adapting any of the more comprehensive recovery scales . Postoperative quality of recovery scale (PostopQRS) is a relatively new recovery score, which was first published on 2010, and was designed to be a tool for assessment of multiple domains in recovery. In this assessment tool, recovery was defined as return to the pre-surgery base line scores or better. The aim of this prospective study is to evaluate the recovery after cesarean section in patients who will receive Quadratus Lumborum Block QLB as a part of multimodal analgesia using Postoperative quality of recovery scale.

Registry
clinicaltrials.gov
Start Date
April 1, 2018
End Date
October 1, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) physical status II, normal singleton pregnancy, 37 weeks gestation or more Scheduled for elective cesarean section

Exclusion Criteria

  • Patients refusing spinal
  • Patients with BMI \>35 kg/m2).
  • Expected difficult surgery (\> 3 previous sections, abnormal placentation, prolonged surgery more than 2 hours from skin to end) and Estimated Blood Loss more than 1500).
  • Expected difficult spinal anesthesia.
  • Abnormal coagulation and other contraindications for spinal anesthesia and/or QLB
  • Patient with chronic pain.
  • Patient treated from psychosis.
  • Patients with communication, language barriers .

Outcomes

Primary Outcomes

change from baseline postoperative quality of recovery score

Time Frame: 72 hours

Domains of postoperative recovery score are : 1. The physiologic domain . 2. The nociceptive domain 3. The emotive domain . 4. Activities of daily living 5. Cognitive domain 6. Over all patients perspective domain

Study Sites (1)

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