# Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.

> **NCT03027661** · PHASE3 · COMPLETED · sponsor: **University of Tennessee** · enrollment: 41 (actual)

## Conditions studied

- Pain, Postoperative

## Interventions

- **DRUG:** Bupivacaine
- **DRUG:** 0.9% Sodium Chloride

## Key facts

- **NCT ID:** NCT03027661
- **Lead sponsor:** University of Tennessee
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2017-08-01
- **Primary completion:** 2018-06-30
- **Final completion:** 2018-06-30
- **Target enrollment:** 41 (ACTUAL)
- **Last updated:** 2018-11-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03027661

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03027661, "Para-cervical Block Prior to Laparoscopic Hysterectomy as an Adjuvant Treatment to Reduce Postoperative Pain.". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT03027661. Licensed CC0.

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