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Study of the effect of plasma rich in growth factors with tunnel technique in the treatment of gingival recession

Study of the effect of plasma rich in growth factors with tunnel technique in the treatment of gingival recession

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100427003813N9
Enrollment
10
Registered
2018-10-02
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-11-05

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

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: At least 18 years old The presence of single-ended gingival recession of the miller class I / II with a depth of 2 mm = <CEG of the anterior and permoral teeth alive teeth, without filling or bleeding of probing (The confounding factor is as low as possible) Ability to maintain proper sanitation(O'LEARY plaque score<=20%) Keratinized gum width greater than 2mm Gingival thickness 0.5 = <2mm apical gum margin Signature of consent form

Exclusion criteria

Exclusion criteria: Pregnancy Coagulation problems Use medications of Platelet Interaction (NSAIDs) Use of drugs which interact with wound healing Any local or systemic disease that has a contraindication to periodontal treatment. Allergy to surgical materials (The confounding factor is as low as possible) Active infectious disease (hepatitis, tuberculosis and AIDS) smoking Fernum stretch in the surgical area Use of traumatic brushing techniques, toothbrushes and abrasive toothbrushes Use of removable prosthesis plaques in the desired area

Design outcomes

Primary

MeasureTime frame
Keratinized tissue width. Timepoint: before surgery, 6 weeks and 3 months after surgery. Method of measurement: with periodontal probe.;Clinical attachment level. Timepoint: before surgery, 6 weeks and 3 months after surgery. Method of measurement: with periodontal probe.;Recession width. Timepoint: before surgery, 2 weeks and 3 months after surgery. Method of measurement: with periodontal probe.;Vertical Recession Depth. Timepoint: before surgery, 2 weeks and 3 months after surgery. Method of measurement: with periodontal probe.;Healing index. Timepoint: 1 and 3 days 1 week and 1 months after surgery. Method of measurement: with healing index (HI) based on Landry index.;Clinical Probing Depth. Timepoint: before surgery, 6 weeks, 3 months after surgery. Method of measurement: with periodontal probe.;Esthetic Visual Analogue scale. Timepoint: before surgery, 6 weeks, 3 months after surgery. Method of measurement: with Visual analogue scale.;Pain Visual Analogue scale. Timepoint: 1, 3 and 7 days after surgery. Method of measurement: whit Visual analogue scale.;Distance from cementoenamel junction (CEJ) to mucogingival junction (MGJ or MGJL) in the middle of the buccal surface of the tooth. Timepoint: before surgery, 6 weeks, 3 months after surgery. Method of measurement: with periodontal probe.;Percentage of Root Coverage. Timepoint: 3 months after surgery. Method of measurement: [(Vertical Recession Depth before surgery - Vertical Recession Depth after Surgery)/ divided Vertical Recession Depth before surgery]*100.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloofar Jenabian

Babol University of Medical Sciences

n.jenabian@mubabol.ac.ir+98 11 3220 7918

Outcome results

None listed

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