Hemorrhage Clinical Trial
Official title:
Non-interventional Trial About Treatment of Haemorrhages in Cholecystectomy With TachoSil (TC-027-DE)
| Verified date | August 2008 |
| Source | Nycomed |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Germany: Ethics Commission |
| Study type | Observational |
- Effectiveness and reliability of TachoSil in cholecystectomy (elective and acute)
- Evaluation of TachoSil in laparoscopic cholecystectomy
- Risk profile of patient under anticoagulant therapy undergoing acute cholecystectomy
- Pharmaco-economic evaluation
- Recording of AE's/SAE's Considering the total number of cholecystectomies in Germany
(170.000 cases/y), out of them about 75% laparoscopic and 10.000 conversions totally it
seems urgent to record data about usage of TachoSil in such procedures. For the time
being TachoSil is applied in about 2% of the gall bladder procedures.
Aim is to evaluate a possible patient and procedure profile where TachoSil is most
beneficial.
| Status | Completed |
| Enrollment | 500 |
| Est. completion date | July 2008 |
| Est. primary completion date | June 2008 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patients undergoing elective or acute cholecystectomy - The only restrictions of use will be those resulting from the contraindications (see section 4.3 of the Summary of Product Characteristics) |
Observational Model: Case Control, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Denmark | Nycomed | Roskilde |
| Lead Sponsor | Collaborator |
|---|---|
| Nycomed |
Denmark,
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