Soap Versus Normal Salin Plus Povidone-iodine in Ununion Wound
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|ClinicalTrials.gov Identifier: NCT01619137|
Recruitment Status : Unknown
Verified October 2012 by Aida Najafian, Hormozgan University of Medical Sciences.
Recruitment status was: Recruiting
First Posted : June 14, 2012
Last Update Posted : October 10, 2012
|Condition or disease||Intervention/treatment||Phase|
|Wound||Drug: water and soap Drug: Povidone-iodine And normal salin treatment||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Investigator)|
|Official Title:||Comparison of the Effect of Water and Soap Irrigation With With Povidone-iodine And Normal Salin Treatment of Patients With Ununion Laparatomy or Episiotomy Wound ( a Pilot Study)|
|Study Start Date :||August 2011|
|Estimated Primary Completion Date :||October 2012|
|Estimated Study Completion Date :||October 2012|
Active Comparator: Povidone-iodine And normal salin
40 patients with complaint of ununion wound of laparatomy or episiotomy coming to Gynecologist`s office or hospital enrolled to this study randomly recieve Povidone-iodine And normal salin treatment.
Drug: Povidone-iodine And normal salin treatment
use of Povidone-iodine And normal salin treatment for irrigation of ununion laparatomy or episiotomy wound.
Active Comparator: water and soap
40 patients coming to Gynecologist`s offices or hospital with complaint of ununion wound of laparatomy or episiotomy in Bandarabbas enrolled to this study and randomly recieve water and soap to irrigation of the wound (it`s not require to be at hospital), washing is for each 6-8 hours per day. and if not difference seen after 4 day, treatment change to Povidone-iodine And normal salin.
Drug: water and soap
water and soap for 6-8 hours per day.
- number of admission day [ Time Frame: 1 month ]number of days the patients in each group admitted in hospital
- complication of each treatment [ Time Frame: 1 months ]complications include of : infection, reopening of wound, and measurment of opening of wound.
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): NCT01619137
|Contact: Aida Najafian, Specialistemail@example.com|
|Iran, Islamic Republic of|
|Bandarabbas, Hormozgan, Iran, Islamic Republic of|
|Contact: Aida Najafian, specialist +989133090692 firstname.lastname@example.org|
|Principal Investigator: Aida Najafian, specialist|
|Principal Investigator:||Aida Najafian||Hormozgan University of Medical Science (HUMS)|