Uterine Cervical Dysplasia Clinical Trial
Official title:
Is a Hemostatic Procedure Required After Biopsy of the Cervix Uteri in Women Undergoing Colposcopy for Cervical Dysplasia? A Multicenter Randomized Non-inferiority Trial
Cytological abnormalities of the Cervix uteri need to be clarified by colposcopy biopsy. To avoid bleeding after biopsy, monsel´s paste is a common used Agent. In a randomized clinical Trial the use of monsel´s paste after biopsy will be compared to no Intervention. The Primary outcome of the study is blood loss, secondary outcomes are pain, satisfaction of the patient and influence of Independent factors such as Age and Body mass index.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01505920 -
Lidocaine Spray Compared With Submucosal Injection During LEEP: a Randomized Controlled Trial
|
Phase 3 | |
Completed |
NCT01014026 -
Self-sampling and Human Papillomavirus (HPV)-Testing for Unscreened Women in Cervical Cancer Prevention
|
Phase 3 | |
Completed |
NCT00377845 -
Cervix Cytological Screening - Comparison of Tampon Self-Test and the Routine Smear.
|
Phase 0 | |
Completed |
NCT02910388 -
LLETZ Under Direct Colposcopic Vision
|
N/A | |
Completed |
NCT00596258 -
A Two-Stage Phase 2 Study Of A-007 Topical Gel in High-Grade Squamous Intraepithelial Lesions (HSIL)
|
Phase 2 | |
Completed |
NCT03763565 -
Effectiveness of HPV Vaccine in Thai Adult Women
|
||
Completed |
NCT04415840 -
Lugol's Solution in Addition to Acetic Acid During Colposcopy
|
||
Recruiting |
NCT04783805 -
Conservative Management of HSIL in Patients With Future Pregnancy Aspiration
|
||
Completed |
NCT04326049 -
LLETZ With Videocolposcopy Versus LLETZ With Binocular Colposcopy
|
N/A | |
Completed |
NCT02515162 -
Fischer Cone Biopsy Excisor Versus Loop Excision Procedure for Conization
|
N/A | |
Completed |
NCT01405768 -
Buffered Lidocaine for Loop Electrosurgical Excision Procedures (LEEPs)
|
Phase 2 | |
Completed |
NCT00264732 -
A Study of Amolimogene (ZYC101a) in Patients With High Grade Cervical Intraepithelial Lesions of the Uterine Cervix
|
Phase 2/Phase 3 | |
Completed |
NCT03296566 -
The SAFE Study: Satisfaction and Adherence to Follow-Up With Colposcopy Exams
|
N/A | |
Completed |
NCT02346227 -
Impact of AV2 Antiviral Drug on the Treatment of HPV-associated Lesions of the Uterine Cervix
|
Phase 3 | |
Completed |
NCT02330471 -
Forced Versus Spray Coagulation in Women Undergoing LLETZ-conization for Cervical Dysplasia: a Randomized Trial
|
Phase 3 | |
Completed |
NCT01035580 -
Trial on Safety and Pharmacokinetics of Intravaginal Curcumin
|
Phase 1 | |
Completed |
NCT01639820 -
Comparison of Pelvic Lymphadenectomy Versus Isolated Sentinel Lymph Node Biopsy Procedure for Early Stages of Cervical Cancers : a Multicenter Study With Evaluation of Medico-economic Impacts
|
N/A | |
Completed |
NCT00285207 -
Safety and Efficacy of A-007 Topical Gel in the Treatment of High-Grade Squamous Intraepithelial Lesions (HSIL) of the Cervix
|
Phase 2 | |
Recruiting |
NCT05225493 -
HIV Indicator Diseases in Hospital and Primary Care
|
||
Completed |
NCT01034358 -
Immune Response to the Human Papillomavirus Vaccine in Young Women With Inflammatory Bowel Disease
|
Phase 4 |