Investigating The Effect Of Olea Ointment On Cesarean Incision Local Pain And Healing In Mothers After Cesarian Cection

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170203032374N3

Enrollment

Registered

2021-10-10

Start date

2021-10-23

Completion date

Unknown

Last updated

2022-02-07

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

Conditions

The Extent of Local Pain and Repair of Cesarean Section in Referring Mothers. • O85-O92 Complications Predominantly Related To the PuerperiumO86.0 Infection of Obstetric Surgical Wound. Infected Caesarean Section Wound Followimg Delivery

Interventions

Intervention 1: Intervention group: The Intervention Group Will Be The Group Receiving Olea Ointment. First, The Researcher Will Be Taught How To Use The Ointment For The First Time, And Then The Samp

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Willingness And Satisfaction To Enter The Study Cesarean Delivery In Al-Zahra Educational-Medical Center In Rasht and Langroud Shahid Hosseinpour Hospital Primary And Multi-par Mothers With A History Of Two Cesarean Sections Gestational Age 37 to 42 Weeks Depending On The Ultrasound Or The First Day Of The Last Period Abdominal Incision Of Transverse Type Maximum Rupture Time Of Membran Less Than 12 Hours Minimum Literacy, Have A phone number To follow Absence Of Systemic Diseases Including Diabetes And Cardiovascular Disease Blood Pressure Coagulation Disorders During Or Before Pregnancy No Postpartum Hemorrhage No Blood Transfusion In Surgery Do Not Take Certain Medications That Increase The Risk Of Postpartum Infection

Exclusion criteria

Exclusion criteria: Misuse Of Olea Ointment By Research Units Allergy To Ointment During the Study Concomitant Use Of Other Ointments Or Topical Medications

Design outcomes

Primary

Measure	Time frame
The Extent of Local Pain and Repair of Cesarean Section in The Referring Mothers. Timepoint: The Severity of Pain Before With the Visual Scale of Pain Ruler and The Condition of Abdominal Incision Improvement Are Also Evaluated And Recorded By The Researcher Using The Reeda Scale Before The Intervention, 24 Hours After The First Intervention And On Days 5 And 10 After Cesarean Section. Method of measurement: Visual Analogue Scale (VAS) and Reeda.	—

Measure

Time frame

The Extent of Local Pain and Repair of Cesarean Section in The Referring Mothers. Timepoint: The Severity of Pain Before With the Visual Scale of Pain Ruler and The Condition of Abdominal Incision Improvement Are Also Evaluated And Recorded By The Researcher Using The Reeda Scale Before The Intervention, 24 Hours After The First Intervention And On Days 5 And 10 After Cesarean Section. Method of measurement: Visual Analogue Scale (VAS) and Reeda.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Jafarzadeh kenarsari

Nursing and Midwifery School of Shahid Dr. Beheshti

f.kenarsari2013@gmail.com+98 13 3355 5058

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026