RecruitingACTRN12625000850471

Effectiveness of Pudendal Nerve Block in reducing Post-Op Pain after Proctological Interventions in patients aged 18 to 70 years old


Sponsor

Combined Military Hospital Tamiz ud din road Rawalpindi Pakistan 46000

Enrollment

96 participants

Start Date

Jul 25, 2024

Study Type

Interventional

Conditions

Summary

Patients were randomized in a 1 : 1 ratio in to two groups A and B. Group A was to receive the pudendal nerve block and group B, not. Effects of pudendal block observed in patients post operatively helping in assessments of post operative pain reduction and additional need of analgesic.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 70 Yearss

Inclusion Criteria1

  • All patients of ages 18 to 70 years, who were declared fit in American Association of Anesthesiologists (ASA) class I or II, for the proctological surgery including hemorrhoidectomy or fistulectomy were enrolled in the trial.

Exclusion Criteria1

  • None

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Interventions

Patients were draped using aseptic technique in the lithotomy position and scrubbed. After the completion of surgery whether for hemorrhoids or anal fistula, the anatomical landmarks were identified f

Patients were draped using aseptic technique in the lithotomy position and scrubbed. After the completion of surgery whether for hemorrhoids or anal fistula, the anatomical landmarks were identified for Pudendal Nerve block for Group A patients. The agents used for the block were 5 ml of 2% Lignocaine mixed with 10 ml of 0.5% Bupivacaine. Trans perineal approach was used for the block. A 25 Gauge, 10 cm, short bevel Spinal Needle was inserted perpendicular to the skin medial to the ischial tuberosity and advanced in the sagittal plane. The confirmation of needle position in proximity of the Pudendal nerve was made upon the slight contraction of the anal sphincter. The anesthetic agents were then injected. Patients were later on shifted to the post operative ward and monitored for pain for 8 hours post surgery. Group B "control" group did not receive any anesthetic. Direct observation and Numeric rating scale was used for pain levels measurement.


Locations(1)

Punjab, Pakistan

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