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Completed

NCT Number: NCT03516786

Quality of Recovery After Quadratus Lumborum Block for Cesarean Section.

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.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Corniche Hospital

Abu Dhabi, 3788, United Arab Emirates

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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 .

Treatment and study plan

Primary outcomes

  1. change from baseline postoperative quality of recovery score

    Time frame: 72 hours

    Domains of postoperative recovery score are :

    • The physiologic domain .
    • The nociceptive domain
    • The emotive domain .
    • Activities of daily living
    • Cognitive domain
    • Over all patients perspective domain

Sponsors and collaborators

Lead sponsor

Corniche Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
May 4, 2018
Registry last updated
Sep 16, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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