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Effect of Coe-Pak Dressing on the Side Effects of Periodontal Surgery

Clinical Trial Study of Coe-Pak Dressing effect on Pain and Microbial Contamination of Suture after Surgery in Patients with Chronic Periodontitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201504114877N26
Enrollment
23
Registered
2015-10-02
Start date
2010-07-23
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: Intervention group: after mixing the equal length of two paste (accelerator paste and base paste), Surgical flaps were covered with uniform pink color of Coe-Pak periodontal dressing (
Treatment - Other
Intervention group: after mixing the equal length of two paste (accelerator paste and base paste), Surgical flaps were covered with uniform pink color of Coe-Pak periodontal dressing (GC Company, Amer
Control group: Surgical flaps were not covered with any periodontal dressing.

Sponsors

Vice Chancellor of Research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with chronic periodontitis disease which require modified widman flap surgery in two quadrants; age over 18 years; lack of systemic disease; no pregnancy; no previous periodontal treatment and systemic antibiotics therapy in the last 6 months; not being smoker. Exclusion criteria: the patient’s unwillingness to continue the treatment; being under other treatment and taking medications which may affect the result during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pain after surgery. Timepoint: 1 week after the surgery. Method of measurement: Visual analog scale questionnaire.;Number of bacterial colonies of sutures after surgery. Timepoint: 1 week after the surgery. Method of measurement: McFarland technique with colony- forming units per milliliter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Jaber Yaghini

Periodontal department, School of Dentistry, Isfahan University of Medical Sciences

j_yaghini@dnt.mui.ac.ir.+98 317922825

Outcome results

None listed

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