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A randomized controlled trial to evaluate the efficacy of Pelvic plexus block in pain reduction during the biopsy of prostate

Pelvic plexus block: An endeavour to reduce pain during transrectal ultrasound guided biopsy of the prostate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/07/004731
Enrollment
139
Registered
2014-07-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Patients with an abnormal prostate on a digital rectal examination and/or serum prostate specific antigen more than 4 ng/ml were included in the study.

Interventions

Intervention1: Pelvic plexus block: 5 ml of 25 lignocaine injection was given on each side into the pelvic neurovascular plexus, situated lateral to the tip of the seminal vesicles under colour Dopple

Sponsors

Tarun Jindal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with an abnormal prostate on a digital rectal examination and/or serum prostate specific antigen (PSA) of > 4 ng/ml were included in the study.

Exclusion criteria

Exclusion criteria: Those who have had a previous transrectal prostate biopsy, chronic prostatitis/pelvic pain, neurological conditions, bleeding diathesis, anticoagulation/antiplatelet therapy, active UTI, haemorrhoids/ anal fissure/ anal fistula, known allergy to lignocaine were excluded from the study.

Design outcomes

Primary

MeasureTime frame
The effect of pelvic plexus block as compared to the pei prostatic block and placebo on the pain during prostate biopsyTimepoint: The evaluation of pain using the visual analogue scale will be made at two pints: 1) During the biopsy 2) 30 minutes following the biopsy

Secondary

MeasureTime frame
The complications occuring due to the biopsy procedureTimepoint: The patients were observed for 2 hours after the procedure.The patients were reviewed again at the end of two weeks to assess the late complication rate.

Countries

India

Contacts

Public Contacttarun jindal

Calcutta National Medical College

drtarunjindal@gmail.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026