Skip to content

Effect of ANGIPARS drug on treatment of gum disease.

Comparison of ANGIPARS and placebo on enhancement of nonsurgical periodontal treatment outcome in moderate to severe periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201307248898N2
Enrollment
46
Registered
2014-07-12
Start date
2013-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Periodontitis. Chronic Periodontitis

Interventions

Intervention 1: Semelil, oral 100mg capsules, twice daily for 3 months. Intervention 2: Placebo in the form of oral capsules, twice daily for 3 months.
Treatment - Drugs
Placebo
Semelil, oral 100mg capsules, twice daily for 3 months
Placebo in the form of oral capsules, twice daily for 3 months

Sponsors

Research Center, Dental School of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion Criteria: moderate to severe generalized chronic periodontitis patients Exclusion Criteria: moderate to severe generalized chronic periodontitis patients with history of systemic disorders ( DM, Cancer, Immune system disorders, bone metabolic disorders, diseases affecting healing potential, radiotherapy history, immunosuppressive treatments); Smoking; Pregnancy or lactation; Taking systemic antibiotics within 2 months; Taking long-term NSAIDs; Periodontal treatments within 1 year

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Plaque Index. Timepoint: Before intervention and 3 months after invertion. Method of measurement: Visual evaluation and periodontal probe.;Modified Gingival Index. Timepoint: before intervention and 3 months after invertion. Method of measurement: Visual evaluation.;Modified Sulcular Bleeding Index. Timepoint: before intervention and 3 months after invertion. Method of measurement: Periodontal probe.;Probing Depth. Timepoint: before intervention and 3 months after invertion. Method of measurement: Periodontal probe.;Clinical Attachment Level. Timepoint: before intervention and 3 months after invertion. Method of measurement: periodontal probe.;8-hydroxy2-deoxyguanosine level. Timepoint: before intervention and 3 months after invertion. Method of measurement: colorimetric measurement in 450 nm with ELIZA kit.;IL-1ß level. Timepoint: before intervention and 3 months after intervention. Method of measurement: optical density measurement in 450 nm with ELIZA kit.;Lipid peroxidation level. Timepoint: before intervention and 3 months after intervention. Method of measurement: optical density measurement of TBARS in 530-535 nm with ELIZA kit.

Secondary

MeasureTime frame
White lesions in oral mucosa. Timepoint: after intervention every 4 weeks. Method of measurement: Visual evaluation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mojgan Paknejad

Dental School of Tehran University of Medical Sciences

mpaknejad@sina.tums.ac.ir+98 21 8835 1170

Outcome results

None listed

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