NCT Number: NCT00242437
Hemostatic Matrix in Endoscopic Sinus Surgery
Evaluating clinical performance of Hemostatic Matrix with bovine thrombin in achieving hemostasis in patients undergoing endoscopic sinus surgery.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
The Summit Medical GroupDepartment of Otolaryngology, Summit, New Jersey, United States
Who can participate
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients who are 18 years or older.
- Patients undergoing elective primary or re-do endoscopic sinus surgery for chronic sinusitis with bleeding surface requiring an adjunct to achieve hemostasis.
- Patients must be willing and capable of cooperating to the extent and degree required by the protocol and sign the IRB approved Informed Consent Form prior to any participation in the study.
Exclusion criteria
- Patients with bleeding diathesis, pathologic coagulopathy, systemic disorders, inflammatory conditions (other than chronic sinusitis or nasal polyposis) or autoimmune, immunodeficiency diseases or any other disorder that may interfere with hemostasis.
- Patients with severe (brisk or forceful) bleeding site(s).
- Patients undergoing urgent or emergency endoscopic sinus surgery.
- Patients with bronchial asthma who have aspirin intolerance.
- Patients with diffuse polyposis that would require chronic oral steroids or patients on chemotherapeutic agents that might delay healing (short term pulse steroid therapy and topical steroids are acceptable).
- Patients who have used anticoagulant, antiplatelet or nonsteroidal anti-inflammatory analgesic (NSAID) within 7 days prior to surgery.
- Patients who are morbidly obese (Body Mass Index > 35).
- Patients with acute local infection at the operative side.
- Patients who are current alcohol and/or drug abusers.
- Patients with neoplasm, craniofacial abnormalities (e.g. cleft palate), or sleep apnea using nasal CPAP, or patients that may require a Lothrop procedure.
- Female patients who are pregnant or nursing.
- Patients who have uncontrolled diabetes mellitus (blood glucose levels >400 mg/dl) as determined by the Investigator based on medical history.
- Patients who have participated in another investigational drug or device research within 30 days of enrollment.
- Patients with known antibodies to bovine thrombin preparations, sensitivities or religious prohibitions to porcine gelatin or bovine components.
Treatment and study plan
bovine thrombin
DevicePrimary outcomes
-
Success in achieving hemostasis after product application
Secondary outcomes
-
Post operative healing
-
Patient Satisfaction
-
Time to hemostasis
Sponsors and collaborators
Lead sponsor
Ethicon, Inc.
Industry
Registry information
Official study title
A Prospective, Multicenter Study to Evaluate Hemostatic Matrix With Bovine Thrombin in Achieving Hemostasis in Patients Undergoing Endoscopic Sinus Surgery
Important dates
- Study start
- 2005
- Study completion
- 2006
- First posted
- Oct 20, 2005
- Registry last updated
- Jul 13, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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