Diplen LX membrane and Coe-pack usage from the patient preference point of view and on the pain and wound healing

The comparison of Diplen LX membrane and Coe-pack usage from the patient preference point of view and on the pain and wound healing after the periodontal flap surgery in patients with moderate to severe periodontitis

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20100412003690N10

Enrollment

Registered

2019-10-30

Start date

2019-06-22

Completion date

Unknown

Last updated

2019-11-05

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

Conditions

Pain after surgery. Pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: All patients complete the first phase of periodontal treatment and are evaluated two weeks after the first phase of treatment. Only those with an index plaque less

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Moderate to severe periodontitis Consent to participate in the study Under 20 percents plaque index Depth of probing envelope greater than 5 mm

Exclusion criteria

Exclusion criteria: Pregnant and lactating women Smokers Minor peridontitis

Design outcomes

Primary

Measure	Time frame
Pain after surgery. Timepoint: 3, 7 and 14 days after intervention. Method of measurement: Visual Analogue Scale.;Wound healing after surgery. Timepoint: 7 and 14 days after intervention. Method of measurement: Wound healing index.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoomeh Faramarzie

Tabriz University of Medical Sciences

faramarzim@tbzmed.ac.ir+98 41 1385 4863

Outcome results

None listed

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