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.
Conditions
Interventions
Sponsors
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
| Measure | Time 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
| Measure | Time 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
Calcutta National Medical College