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Clinical Trials/NCT05514977
NCT05514977UnknownNot Applicable

Ultrasound Guided Thoracic Erector Spine Plane Block for Post Mastectomy Pain Control, Effect of Volume With Constant Drug Mass, a Randomized Controlled Trial

Cairo University1 site in 1 country82 target enrollmentStarted: September 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
82
Locations
1
Primary Endpoint
Effective analgesia

Study Overview

Brief Summary

The investigators compare 2 different drug regimens using 2 different volumes of lidocaine with the same drug content (i.e. different concentrations) as regards efficacy of post operative analgesia following mastectomy surgery

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ASA 2 & 3 for elective breast cancer surgery

Exclusion Criteria

  • BMI > 35 kg/m2
  • Contraindications to LA (coagulopathy and local infection)
  • Allergy to the drug
  • Cardiac, hepatic and renal patients

Outcomes

Primary Outcomes

Effective analgesia

Time Frame: First 24 hours

Morphine supplements needed

Secondary Outcomes

  • Analgesic efficiency(Every 2 hours in the first 24 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Kareem

Assistant professor

Cairo University

Study Sites (1)

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