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Clinical Trials/NCT05172882
NCT05172882
Completed
N/A

Comparison of the Efficacy of Transversalis Fascia Plane Block and Wound Infiltration in Varicoselectomy Surgery; Randomised, Controlled Study.

Ataturk University1 site in 1 country60 target enrollmentNovember 15, 2021
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ConditionsAnalgesiaTransversalis Fascia Plane BlockWound InfiltrationVaricoselectomy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Analgesia
Sponsor
Ataturk University
Enrollment
60
Locations
1
Primary Endpoint
Pain Scores (0 (low)-10 (high))
Status
Completed
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

Before surgery, patients will be divided into 2 groups as transversalis fascia plane block will be applied and skin infiltration will be applied. Post-operative analgesic procedures will be applied to patients receiving general anesthesia. Postoperative analgesic consumption and pain scores of the patients will be evaluated.

Registry
clinicaltrials.gov
Start Date
November 15, 2021
End Date
April 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Erkan Cem ÇELİK

Associate Professor

Ataturk University

Eligibility Criteria

Inclusion Criteria

  • •Patients over the age of 18 who will undergo Varicocele operation

Exclusion Criteria

  • •Patients with allergic reaction to anesthesia and analgesia drugs to be used
  • •Patients who did not want to voluntarily participate in the study
  • •Severe systemic disease (kidney, liver, pulmonary, endocrine)
  • •Substance abuse history
  • •Chronic pain history
  • •Psychiatric problems and communication difficulties
  • •History of hematological problem
  • •Patients with severe hemodynamic instability due to infection, heavy bleeding

Outcomes

Primary Outcomes

Pain Scores (0 (low)-10 (high))

Time Frame: 24th hour

Pain will be assessed by visual analog scale scores

Secondary Outcomes

  • Rescue analgesic consumption(Any time on postsurgical first 24 hour.)

Study Sites (1)

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