Prophylactic Antibiotic Treatment During Vaginal Repair
The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2005 by Hvidovre University Hospital.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Hvidovre University Hospital
Information provided by:
Hvidovre University Hospital
ClinicalTrials.gov Identifier:
NCT00162604
First received: September 9, 2005
Last updated: September 8, 2006
Last verified: February 2005
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Purpose
Prolapse of the uterus, bladder and rectum is a common condition in multiparous and/or elderly women. The number of operations for vaginal repair is increasing in Denmark, but there is no consensus or evidence found about the efficiency of prophylactic antibiotics intraoperatively concerning postoperative infections.
The objective of this randomized, controlled trial is to investigate the significance of prophylactic antibiotic treatment in vaginal repair operations.
| Condition | Intervention |
|---|---|
|
Uterine Prolapse Cystocele Rectocele Enterocele |
Drug: Cefuroxime |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double-Blind Primary Purpose: Prevention |
| Official Title: | Antibiotikaprofylakse Ved Vaginalplastik |
Resource links provided by NLM:
Further study details as provided by Hvidovre University Hospital:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Women ages 18+ with uterine prolapse grade I - II and/or cystocele and/or rectocele and/or enterocele grade I - II and/or defects of the perineal body, in whom there is medical indication for vaginal repair, but no indication for vaginal hysterectomy or transvaginal suspension of the vaginal vault after prior hysterectomy.
Exclusion Criteria:
- Patients allergic to cefuroxime.
- Patients in whom a vaginal hysterectomy or a transvaginal suspension of the vaginal vault or other major surgery is planned, where prophylactic antibiotic treatment is standard.
- Patients suffering from physical or mental disorders that will not allow them to give informed consent.
- Pregnant and nursing women.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00162604
Contacts
| Contact: Marianne Ottesen, M.D | 0045 36323632 ext 3540 | marianne.8sen@dadlnet.dk |
Locations
| Denmark | |
| Hvidovre University Hospital | Recruiting |
| Hvidovre, Denmark, 2650 | |
| Contact: Marianne Ottesen, M.D 0045 36323632 ext 3540 marianne.8sen@dadlnet.dk | |
| Sub-Investigator: Tina Olsen, M.D | |
| Sub-Investigator: Abelone Elisabeth Sakse, M.D | |
| Principal Investigator: Marianne Ottesen, M.D, PhD | |
Sponsors and Collaborators
Hvidovre University Hospital
Investigators
| Study Director: | Marianne Ottesen, M.D, Ph.D | Hvidovre University Hospital |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00162604 History of Changes |
| Other Study ID Numbers: | 2602-415 |
| Study First Received: | September 9, 2005 |
| Last Updated: | September 8, 2006 |
| Health Authority: | Denmark: Danish Medicines Agency |
Keywords provided by Hvidovre University Hospital:
|
Prophylactic antibiotic Postoperative infections Uterine prolapse grade I - II cystocele |
rectocele enterocele defects of the perineal body |
Additional relevant MeSH terms:
|
Cystocele Prolapse Uterine Prolapse Rectocele Hernia Urinary Bladder Diseases Urologic Diseases Pelvic Organ Prolapse Pathological Conditions, Anatomical Uterine Diseases Genital Diseases, Female |
Rectal Diseases Intestinal Diseases Gastrointestinal Diseases Digestive System Diseases Anti-Bacterial Agents Cefuroxime Cefuroxime axetil Anti-Infective Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013