drugset / Trial / NCT01224145
Assess the Feasibility and Efficacy of the CollaRx® Bupivacaine Implant Laparoscopic Inguinal or Umbilical Herniorrhaphy
NaSingle-groupOpen-labelTreatment
Summary
This study will assess pain intensity for the first 72 hrs after aggravated movement (cough) following Laparoscopic Inguinal or Umbilical Herniorrhaphy.
Timeline
- Start
- 2011-03-22
- Primary completion
- 2011-06-20
- Completion
- 2011-06-20
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bupivacaine | Other / unclassified | 200 mg | — |
Indications
No indication recorded.