Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

The Effect of Clamping the Indwelling Urethral Catheter Before Removal From Patients After Type III Radical Hysterectomy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02083614
Recruitment Status : Unknown
Verified March 2014 by Yao Gong, First Affiliated Hospital of Chongqing Medical University.
Recruitment status was:  Recruiting
First Posted : March 11, 2014
Last Update Posted : March 11, 2014
Sponsor:
Information provided by (Responsible Party):
Yao Gong, First Affiliated Hospital of Chongqing Medical University

Brief Summary:
The effect of clamping the indwelling urethral catheter before removal is an unsettled issue in clinical practice. No studies have done before in the patients with gynecologic cancers who received radical hysterectomy. We hypothesized that clamping the catheter would decrease the rate of recatheterization. In addition, the feeling of urination during clamping is correlated with lower rate of recatheterization after removal.

Condition or disease Intervention/treatment Phase
Gynecologic Cancer Procedure: to clamp or release the catheter for 2 days before removal Not Applicable

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Study Start Date : November 2013
Estimated Primary Completion Date : November 2014
Estimated Study Completion Date : November 2015

Arm Intervention/treatment
Experimental: clamping
to clamp or release the catheter for 2 days before removal
Procedure: to clamp or release the catheter for 2 days before removal
No Intervention: no clamping



Primary Outcome Measures :
  1. rate of recatheterization [ Time Frame: 12 months ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • patients receiving Piver III radical hysterectomy
  • catheterization over 7 days

Exclusion Criteria:

  • catheterization shorter than 7 days

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02083614


Contacts
Layout table for location contacts
Contact: fulan wang 00862389011080 wfl3076@163.com
Contact: ling zhao 00862389011006 239648507@qq.com

Locations
Layout table for location information
China
Fulan Wang Recruiting
Chongqing, China, 400016
Sub-Investigator: ling zhao         
Sponsors and Collaborators
First Affiliated Hospital of Chongqing Medical University
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Layout table for additonal information
Responsible Party: Yao Gong, M.D., First Affiliated Hospital of Chongqing Medical University
ClinicalTrials.gov Identifier: NCT02083614    
Other Study ID Numbers: CIUCGY-1
First Posted: March 11, 2014    Key Record Dates
Last Update Posted: March 11, 2014
Last Verified: March 2014