Trials / Terminated
TerminatedNCT01810900
To Assess the Anti-adhesive Effect and Safety of Protescal
To Assess the Anti-adhesive Effect and Safety of Protescal Following Laparoscopic Surgery
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- LG Life Sciences · Industry
- Sex
- Female
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
This multicenter, randomized, single-blind study assessed the safety and efficacy of Protescal for the reduction of post-operative adhesion formation following myomectomy.
Detailed description
The age of the patients participating in the study overed 20 years and included nonpregnant women requiring laparoscopic myomectomy and expected to undergo a second-look laparoscopy as part of their treatment plan 5 weeks after the initial surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Protescal |
Timeline
- Start date
- 2012-09-01
- Primary completion
- 2013-11-01
- Completion
- 2013-12-01
- First posted
- 2013-03-14
- Last updated
- 2016-03-11
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT01810900. Inclusion in this directory is not an endorsement.