Design and formulation of periodontal dressing and invivo assesment incompare with Coe-pak

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

IRCT

Registry ID

IRCT201104131606N6

Enrollment

Registered

2011-05-26

Start date

2011-03-04

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

Periodontal desease. Acute periodontitis

Interventions

Intervention 1: Control group: using co-pack after surgery. Intervention 2: Intervention group: using new formulation after surgery.

Treatment - Drugs

Control group: using co-pack after surgery

Intervention group: using new formulation after surgery

Eligibility

Sex/Gender

All

Age

35 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : Aage between 35- 60 years with periodontal disease. Exclusion criteria: Pregnancy. breast feeding, bleeding and perforation or rapture of gums

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Tssues healing. Timepoint: Daily. Method of measurement: Examination by periodontist.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Jalal Hamissi

Qazvin University of Medical Sciences

jhamissi@qums.ac.ir+98 28 1335 3067

Outcome results

None listed

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