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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05172882
Other study ID # ATATÜRK ÜNIVERSITESI
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 15, 2021
Est. completion date April 15, 2022

Study information

Verified date November 2022
Source Ataturk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date April 15, 2022
Est. primary completion date March 15, 2022
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 70 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Procedure:
Wound site infiltration
Block fluids that were prepared as 20 ml 0.25% bupivacaine before the intervention, will be applied through the upper and lower incision lips on the suprainguinal surgical site.
Transversalis fascia plane block
External, internal oblique, and transversus abdominis muscles will be visualized by the ultrasound device. After transversalis fascia will be seen, transversalis fascia plane block will be performed. As a block fluid 20 ml 0.25% bupivacaine will be applied.

Locations

Country Name City State
Turkey Erkan Cem ÇELIK Erzurum

Sponsors (1)

Lead Sponsor Collaborator
Ataturk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 1st hour
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 2nd hour
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 4th hour
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 8th hour
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 12th hour
Primary Pain Scores (0 (low)-10 (high)) Pain will be assessed by visual analog scale scores 24th hour
Secondary Rescue analgesic consumption Analgesic drug consumption will be assessed Any time on postsurgical first 24 hour.
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