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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03537313
Other study ID # RJVAG001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 15, 2018
Est. completion date September 30, 2018

Study information

Verified date May 2018
Source Rajavithi Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison of the effectiveness of povidone-iodine douching and painting for reducing febrile morbidity after total abdominal hysterectomy


Description:

Total abdominal hysterectomy (TAH) is the most common gynecologic operation worldwide. The two most common complications after TAH are febrile and infectious morbidities, incidence varying between 5 and 50 percent. After performing TAH, vaginal canal must be breached and closed to be blind-pouch stump. Routing vaginal douching at the night before and on the morning of the surgical date, and intra-operative painting are routinely practiced. However, no good quality of evidence base supports the effectiveness of vaginal douching and painting in preventing febrile and infectious morbidities after TAH.


Recruitment information / eligibility

Status Completed
Enrollment 300
Est. completion date September 30, 2018
Est. primary completion date September 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Women who undergoing total abdominal hysterectomy - Woman who agrees to participate in this study Exclusion Criteria: - Women with history of sea-food or iodine allergy - Women who undergo emergency TAH - Women who have intestinal resection in this operation - Women who have active pelvic inflammatory disease before operation - Women who have fever before operation - Women who received antibiotic within 1 weeks before operation - Women who be immunocompromised host

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Vagina douching
Vaginal douches with 1000 ml of 1% povidone-iodine solution on the night before surgery and again on the morning of surgery
Vagina painting
Vaginal painting of vagina stump after hysterectomy with 10% povidone-iodine solution 30 ml

Locations

Country Name City State
Thailand Rajavithi hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Rajavithi Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Febrile morbidity Defined as the presence of an oral temperature > 38 o C (100.4 o F) on two occasions at least 4 hours apart in the post-operative period excluding the first 24 hours Day 1-7 after surgery
Secondary Vaginal cuff infection Defined as redness, tenderness, infiltration or abscess at vaginal cuff 2 weeks after surgery
Secondary Other infectious morbidities Defined by the presence of a urinary tract infection, abdominal wound infection, or pneumonitis; urinary tract infection defined as symptomatic infection with a mid-steam urine specimen showed bacterial growth > 105 bacteria/ml of urine; surgical wound infection defined as redness, tenderness, infiltration or abscess; pneumonitis defined as fever, physical and radiological findings of consolidation 2 weeks after surgery
See also
  Status Clinical Trial Phase
Completed NCT00845754 - Post-Operative Treatment With Ketorolac After Abdominal Myomectomy N/A