Quality of Recovery After Quadratus Lumborum Block for Cesarean Section.

Postoperative Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03516786
• Other study ID #: Ch1712171
• Status: Completed
• Start date: April 1, 2018
• Est. completion date: October 1, 2019

Study information

• Verified date: September 2020
• Source: Corniche Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: October 1, 2019
• Est. primary completion date: September 15, 2019
• Gender: Female
• Age group: 18 Years to 45 Years

Eligibility

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 .

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Locations

Country	Name	City	State
United Arab Emirates	Corniche Hospital	Abu Dhabi

Sponsors (1)

Lead Sponsor	Collaborator
Corniche Hospital

Country where clinical trial is conducted

United Arab Emirates, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	change from baseline postoperative quality of recovery score	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	72 hours