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Effect of bistort mouthwash on pregnancy gingivitis

Comparison of the effect of bistort mouthwash with chlorhexidine mouthwash on periodontal indices and oral health-related quality of life in pregnant women with gingivitis.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241221064118N1
Enrollment
84
Registered
2025-06-14
Start date
2025-08-23
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Pregnancy Gingivitis. Gingivitis and periodontal diseases

Interventions

Intervention 1: Intervention group: Participants in this group will use bistort mouthwash twice daily for 2 weeks after scaling and receiving routine oral hygiene education. Patients should refrain fr

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women from 15 to 28 weeks of pregnancy Aged 15 to 45 years Non-smoker Having gingivitis based on validated periodontal indicators Presence of microbial plaque measured based on scientific indicators If the presence of tooth discoloration is due to a dental infection No need for antibiotic prophylaxis

Exclusion criteria

Exclusion criteria: Use of anti-inflammatory drugs and antibiotics in the past 3 months Nausea and vomiting during pregnancy Having systemic disease Reluctance to cooperate

Design outcomes

Primary

MeasureTime frame
Plaque Index. Timepoint: At baseline and two weeks after the intervention. Method of measurement: Clinically assessed by a trained evaluator using the silness & loe plaque index.;Gingival index. Timepoint: At baseline and two weeks after the intervention. Method of measurement: clinically assessed by a trained evaluator using the loe & silness Gingival index.;Stain Index. Timepoint: At baseline and two weeks after the intervention. Method of measurement: Clinically examined and scored using standard visual methods by trained evaluator.;Oral Health -Related Quality of Life. Timepoint: At baseline and two weeks after the intervention. Method of measurement: Self-reported by participants using the standardized OHIP-14 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh ebrahimi

Mashhad University of Medical Sciences

ebrahimisfpp@gmail.com+98 51 5523 0425

Outcome results

None listed

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