# "Loss of Resistance" Versus CompuFlo® for Epidural Placement

> **NCT00178750** · PHASE1,PHASE2 · WITHDRAWN · sponsor: **The University of Texas Health Science Center, Houston**

## Conditions studied

- Pain
- Epidural Analgesia

## Interventions

- **DEVICE:** 18G Tuohy epidural needle
- **DEVICE:** CompuFlo® computerized syringe pump

## Key facts

- **NCT ID:** NCT00178750
- **Lead sponsor:** The University of Texas Health Science Center, Houston
- **Sponsor class:** OTHER
- **Phase:** PHASE1,PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** —
- **Primary completion:** —
- **Final completion:** —
- **Target enrollment:** 0 (ACTUAL)
- **Why stopped:** Study did not start due to investigator time constraints
- **Last updated:** 2020-11-05


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00178750

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00178750, ""Loss of Resistance" Versus CompuFlo® for Epidural Placement". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT00178750. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*