Treatment of gum loss using blood derived membrane and tissue obtained from palate

Evaluation of the clinical efficacy of platelet rich fibrin obtained through the horizontal spin technique along with coronally advanced flap and connective tissue graft obtained by de-epithelized free gingival graft in the treatment of gingival recession - A Prospective comparative clinical trial - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064826

Enrollment

Registered

2024-03-27

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

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

Conditions

Health Condition 1: K060- Gingival recession

Interventions

Intervention1: Test group: Gingival recession sites treated with coronally advanced flap and platelet rich fibrin obtained by horizontal spin protocol. After treatment patients will be followed for a

Eligibility

Inclusion criteria

Inclusion criteria: 1. Gingival recession defects in maxillary anteriors and premolars (Cairo’s RT1 & RT2 class of recession) 2. Sites with minimum depth of recession =2mm. 3. Isolated or multiple adjoining recession involving =3 teeth.

Exclusion criteria

Exclusion criteria: 1. Sites with probing pocket depth =4mm. 2. Teeth with mobility and/or associated with trauma from occlusion. 3. Sites with dental caries and prosthetic restorations. 4. Patients who exhibit unacceptable oral hygiene compliance during/or after phase ? therapy. 5. Smokers. 6. Pregnant and lactating women. 7. Patients with known platelet disorders or using any medication that are known to interfere with platelet function. 8. Patients with systemic conditions or disease influencing the course of periodontal disease and therapy.

Design outcomes

Primary

Measure	Time frame
1.To assess and compare the changes in the recession height (RH) 2.To assess and compare the percentage of Complete root coverage (CRC%) Timepoint: Baseline and six months	—

Secondary

Measure	Time frame
To evaluate and compare the changes in the following parameters between the study groups before and after therapy 1. Width of keratinised gingiva (WKT) 2. Gingival phenotype Timepoint: baseline and six months	—

Countries

India

Contacts

Public ContactDr Anupama Tadepalli

SRM dental collge

anupamamds@gmail.com9677065517

Outcome results

None listed

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