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NCT05277974 Clinical Trial

Bupivicain vs Bupivicain Plus Dexamethasone in ESP Block for Post-op Analgesia

Post Operative Pain Clinical Trial

Official title:
Comparison of Bupivicain Alone With Bupivicain Plus Dexamethasone in Erector Spinae Plane Block For Post-Operative Analgesia After Thoracotomy

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05277974
Other study ID # ASIDDIQUE SZMC
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date February 15, 2022
Est. completion date July 10, 2022

Study information
Verified date March 2022
Source Sheikh Zayed Medical College
Contact amjad siddique, FCPS
Phone 0689230165
Email dramjadsiddique74@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thoracotomy is a very painful procedure. Different treatment modalities are being utilized for post-thoracotomy analgesia including I/V NSAID, Opoids and Neuropathic medications. Other techniques commonly utilized include Thoracic epidural, Paravertebral block; but both are associated with significant failure rate and other complications. Ultrasound guided Erector Spinae Plane block is a new regional anesthesia technique that provides analgesia at multidermatomal levels acriss the posterior, lateral and anterior thoracic walls. The rational of my study is that it is a novel technique and studies with bupivicain alone are present but no study was found with bupivicain plus dexamethasone.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date July 10, 2022
Est. primary completion date June 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - age 18-60years ASA I-III Patients undergoing elective thoracotomies Exclusion Criteria: - Refusal of Patient Coagulation disorders Known Allergy to Local Anesthetics Infection at the site of injection Pregnant females Morbid Obesity(BMI>40kg/m2) Psychiatric illness Diabetic Patients.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• inj bupivicain
In goup B 30ml of inj. bupivicaine only will be given in Erector Spinae Plane Block and In Group D inj Bupivicain plus inj dexamethasone will be given

Locations
Country Name City State
Pakistan Sheikh Zayed Medical College/Hospital Rahim yar khan Punjab
Pakistan Sheikh Zayed Medical College/Hospital Rahim Yar Khan Rahim yar khan Punjab

Sponsors (1)
Lead Sponsor Collaborator
Sheikh Zayed Medical College

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary postoperative pain scores Visual Analogue Score is utilized to assess the postoperative pain 36 hours postoperatively
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