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Efficacy of Transversalis Fascia Plane Block Versus Wound Infiltration in Varicoselectomy Surgery

Not Applicable
Completed
Conditions
Analgesia
Transversalis Fascia Plane Block
Wound Infiltration
Varicoselectomy
Interventions
Procedure: Wound site infiltration
Procedure: Transversalis fascia plane block
Registration Number
NCT05172882
Lead Sponsor
Ataturk University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
60
Inclusion Criteria
  • Patients over the age of 18 who will undergo Varicocele operation
  • ASA I-II
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Wound InfiltrationWound site infiltrationWound infiltration will be applied to the surgical incision site for patients in this group. Infiltration fluid will contain 20 ml 0.25% bupivakain.
Transversalis Fascia Plane BlockTransversalis fascia plane blockTransversalis fascia plane block will be performed on only one periinguinal side for patients in this group. Block fluid will contain 20 ml 0.25% bupivakain.
Primary Outcome Measures
NameTimeMethod
Pain Scores (0 (low)-10 (high))24th hour

Pain will be assessed by visual analog scale scores

Secondary Outcome Measures
NameTimeMethod
Rescue analgesic consumptionAny time on postsurgical first 24 hour.

Analgesic drug consumption will be assessed

Trial Locations

Locations (1)

Erkan Cem ÇELİK

🇹🇷

Erzurum, Turkey

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