Evaluation the effect of mucous adhesive nifedipine on wound healing in the palate (clinical trials)

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190430043431N1

Enrollment

Registered

2019-06-21

Start date

2018-03-11

Completion date

Unknown

Last updated

2019-08-26

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

Conditions

Gingival recession. Gingival recession

Interventions

Intervention 1: Control group: gingival graft surgery with mucous adhesive. Intervention 2: Intervention group: gingival graft surgery with mucous adhesive nifedipine.

Eligibility

Sex/Gender

All

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients undergoing gingival surgery requiring graft in the palate In the age range of 20 to 50 years

Exclusion criteria

Exclusion criteria: Systemic conditions

Design outcomes

Primary

Measure	Time frame
Landry restoration index. Timepoint: 2, 4, 7, 14, and 30 days after surgery. Method of measurement: by Landry, Turnbull and Howley index.;Pain Visual Analogue scale. Timepoint: 2, 4, 7, 14, and 30 day after surgery. Method of measurement: by Visual Analogue Scale.;Manchester restoration index. Timepoint: 2, 4, 7, 14, and 30 days after surgery. Method of measurement: by Manchester index.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina Motallebnejad

Babol University of Medical Sciences

Mmotallebnejad@mubabol.ac.ir+98 11 3228 9046

Outcome results

None listed

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