Quadratus Lumborum Block III Versus Peritubal Local Infiltration

Postoperative Pain Clinical Trial

Official title:

Postoperative Analgesic Efficiency of Quadratus Lumborum Block III Versus Peritubal Local Infiltration in Patients Undergoing exPercutaneous Percutaneous Nephrolithotomy Operation : a Randomized Comparative Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04215705
• Other study ID #: Post PCNL analgesia
• Status: Completed
• Phase: N/A
• Start date: December 30, 2019
• Est. completion date: July 15, 2020

Study information

• Verified date: November 2020
• Source: Ain Shams University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Investigators compare post operative analgesic efficacy of peritubal local infiltration versus Quadratus Lumborum Block III . In patients undergoing Percutaneous Nephrolithotomy operation

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: July 15, 2020
• Est. primary completion date: July 12, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 21 Years to 70 Years

Eligibility

Inclusion Criteria:

• patient with pelvic renal stone less than 2 cm

• Americans society of Anesthesiologists physical status I, II

• BMI<35

Exclusion Criteria:

• patient refusal to participate in the study

• Americans society of Anesthesiologists physical status III or above

• major hepatic, renal or cardiovascular disease

• BMI > 35

• coagulopathy

• psychological disorders.

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Procedure:
• Quadratus block versus peritubal local infiltration
Quadratus lumborum block III versus peritubal local infiltration in patients undergoing Percutaneous Nephrolithotomy operation

Locations

Country	Name	City	State
Egypt	Ain Shams University hosptal	Cairo	Abbasya

Sponsors (1)

Lead Sponsor	Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative analgesia	Postoperative pain measured by visual analogue scale from 0 to 10 measured over 24h where 0 is better and 10 means worst pain	24 hours
Primary	Analgesic requirement	Investigators measured the total dose of morphine consumption in mg over 24hour	24 hours