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Soap Versus Normal Salin Plus Povidone-iodine in Ununion Wound

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)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01619137
Enrollment
40
Registered
2012-06-14
Start date
2011-08-31
Completion date
2012-10-31
Last updated
2012-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound

Keywords

ununion wound, soap, irrigation, Povidone-iodine, normal salin

Brief summary

Comparison of the effect of water and soap irrigation with Povidone-iodine And normal salin treatment of patients with ununion laparatomy or episiotomy wound ( a pilot study)

Detailed description

IN Comparison of the effect of water and soap irrigation with Povidone-iodine And normal salin treatment of patients with ununion laparatomy or episiotomy wound ( a pilot study), We use soap in one group and Povidone-iodine And normal salin in other group for irrigation of ununion laparatomy or episiotomy wound.it's require the patients in Povidone-iodine And normal salin group be at hospital till wound be able to closed.

Interventions

water and soap for 6-8 hours per day.

DRUGPovidone-iodine And normal salin treatment

use of Povidone-iodine And normal salin treatment for irrigation of ununion laparatomy or episiotomy wound.

Sponsors

Aida Najafian
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
10 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* all the women coming to Shariati hospital or Gynecologist's office with complain of ununion wound of laparatomy or episiotomy enroll to this study

Exclusion criteria

* patients not satisfacted to participant in the study exclude of it

Design outcomes

Primary

MeasureTime frameDescription
number of admission day1 monthnumber of days the patients in each group admitted in hospital

Secondary

MeasureTime frameDescription
complication of each treatment1 monthscomplications include of : infection, reopening of wound, and measurment of opening of wound.

Countries

Iran

Contacts

Primary ContactAida Najafian, Specialist
dr.aidanajafian@yahoo.com+989133090692

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026