Evaluating the safety and effectiveness of Sigol insect repellent spray

Evaluating the safety (safety/harmlessness) and effectiveness of Sigol brand insect repellent spray in healthy volunteer

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150101020514N21

Enrollment

Registered

2023-03-14

Start date

2023-04-19

Completion date

Unknown

Last updated

2023-04-03

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

Conditions

Insect bite (nonvenomous).

Interventions

Intervention 1: Intervention group: 1 ml of Sigol insect repellent a product of Akhavi Laboratory is sprayed on a forearm and after 30 minutes, the treated area is placed in a test cage, and it is ex

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Ages 18 to 60 Signing consent form to participate in the study Observing the study conditions and tendency to attend regular follow-up courses Insensitivity of volunteers to the experimental herbal composition Insensitivity or mild sensitivity to mosquito bites

Exclusion criteria

Exclusion criteria: Documented sensitivity to formulation components susceptibility to mosquito bites active smokers

Design outcomes

Primary

Measure	Time frame
Estimated full protection time (Measurement of repellent application time up to the first mosquito landing or exploration ). Timepoint: A three-minute interval. Method of measurement: Using a digital camera.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAniseh Samadi

Tehran University of Medical Sciences

aniseh_samadi@yahoo.com+98 21 8896 0880

Outcome results

None listed

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