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the effect of aloe vera gel on prevention of SG

Evaluating the effect of aloe vera gel on prevention of SG in nulliparous woman

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190305042927N1
Enrollment
90
Registered
2020-07-26
Start date
2019-06-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Striea gravidarum.

Interventions

Intervention 1: "Intervention group:" Receive aloe vera gel 75% from the 20th week of pregnancy to 28 pregnancies once a day in the amount of 5 grams or the equivalent of approximately 3 fingertips wi

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Nulliparus Single pregnancy Age:20-35 year

Exclusion criteria

Exclusion criteria: History of previous striae in the abdomen History of skin diseases

Design outcomes

Primary

MeasureTime frame
Stria score in the Davy checklist. Timepoint: At the beginning of the study and 8 weeks after the intervention. Method of measurement: Davy method: The number of striae in each quarter of the abdomen is scored: "Score zero, no striae", "score one, number 2 striae", "score two, number 3-3 striae" and a total score of 0-0. . The final evaluation of striae severity is done in three groups: "zero without striae", "2-1 moderate striae" and "3-8 severe striae".;Severity ofstriae pruritus. Timepoint: 8 weeks after the intervention. Method of measurement: It was evaluated by Kamini method with a score of 4-0. Without itching "score 0", mild itching (1-2 times a day) "score 1", moderate itching without disruption of daily work (3-4 times a day) "score 2", severe itching (6- 5 times a day) annoying daily work "score 3" and severe itching throughout the day and disturbing work and sleep "score 4".;Severity of striae erythema. Timepoint: 8 weeks after the intervention. Method of measurement: By the way of Atval Assessed with a score of 3-0: no erythema "score 0", moderate erythema (bright red or pink) "score 1", symptomatic erythema (red) "score 2", severe erythema (purple) "score 3" Was considered.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahar Bagherian

Shahid Beheshti University of Medical Sciences

bagherian.midwife94@gmail.com+98 21 8820 2512

Outcome results

None listed

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