View Clinical Trial (Medical Research Study)
Transvaginal Appendectomy - NCT00806429-06510(Clinical Trial 258674)
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New Haven |
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State:
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CT |
| Zip Code: |
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06510 |
| Conditions: |
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Appendicitis |
| Purpose: |
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The purpose of this study is to determine the feasibility and safety of transvaginal
appendectomy and determine and compare the postoperative pain and quality of life after
surgery to standard laparoscopic transabdominal appendectomy.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- ultrasound or CT-based diagnosis of acute or chronic appendicitis
- ASA classification 1 or 2
Exclusion Criteria:
- BMI >35
- on Immunosuppressive meds or immunocompromised
- on blood thinners or aspirin or abnormal coagulation tests
- h/o ectopic pregnancy, PID or endometriosis
- prior open abdominal surgery or transvaginal surgery
- with diffuse peritonitis
- evidence of abscess
- retroflexed uterus
- non english speaking |
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| Study is available at: |
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Yale-New Haven Hospital New Haven, CT 06510 United States
Primary Contact: Kurt E Roberts, MD Email: kurt.roberts@yale.edu Phone: 2037649060 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 22, 2011 |
Modifications to
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