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Investigating the Effect of hydroalcoholic extract of Clove plants on the Severity of Pain and Episiotomy Wound Healing inPregnant mothers

Investigating the Effect of hydroalcoholic extract of Clove plants on the Severity of Pain and Episiotomy Wound Healing inPregnant mothers

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181216041990N1
Enrollment
146
Registered
2018-12-26
Start date
2019-01-30
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

the Severity of Pain and Episiotomy Wound Healing.

Interventions

Intervention 1: Intervention group: Take 0.25 ml of clove extract in 4 liters of water and leave twice for 30 minutes. Intervention 2: Control group: Place 0.25 ml of the placebo solution in 4 liters

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Age aged 18-35 Have at least read and write Having a natural delivery plan Life with yours Not having an indication for cesarean section Body mass index in range 19.8-29 Embryo unit with Vertex display Having a midwifery history Maternal admission after the 20th week of pregnancy No history of medical and mental illness Rupture of curtains less 10 hours Lack of curettage No history of reconstructive surgery on the vagina and mandarin No use of certain medications

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The Severity of Pain and Episiotomy Wound Healing. Timepoint: Before intervention and On days 3 to 5 and 10 after intervention. Method of measurement: Visual Analogue Scale and REDA.

Secondary

MeasureTime frame
Pain rate. Timepoint: Before the intervention and every 3 to 5 and 10 days after the intervention. Method of measurement: Visual Analogue Scale.;Episiotomy Woud healing. Timepoint: Before the intervention and every 3 to 5 and 10 days after the intervention. Method of measurement: READA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeideh Rajabzadeh

Gonabad University of Medical Sciences

s.rajabzadeh@gmu.ac.ir+98 51 5722 5027

Outcome results

None listed

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