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USE OF INJECTABLE FORMS OF HYALURONIC ACID AND PLATELET RICH FIBRIN IN THE TREATMENT OF GUM LOSS IN BETWEEN TWO TEETH

COMPARISON OF INJECTABLE FORMS OF HYALURONIC ACID AND PLATELET RICH FIBRIN IN THE TREATMENT OF INTERDENTAL PAPILLARY LOSS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029924
Enrollment
20
Registered
2020-12-18
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K053- Chronic periodontitis

Interventions

Intervention1: Hyaluronic acid (HA) is a FDA approved.: Formed by disaccharide units, is non-immunogenic, enzymatically degradable and relatively non adhesive to cells and proteins and capable of inte

Sponsors

Institute of Dental Studies and Technologies
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients in good general health • Patients with at least one Type I or II (Norland and Tarnowâ??s classification)7 deficient papilla in anterior region • Well aligned maxillary teeth, no spacing, no crowding or intrusion or extrusion.

Exclusion criteria

Exclusion criteria: • Pregnant and lactating mothers • History of tobacco consumption. • History of taking any medications which are known to increase the risk of gingival hyperplasia. • Any artificial crown, proximal cervical restoration or abrasion of maxillary anterior teeth. • Any known allergy with hyaluronic acid • Patients with history of traumatic oral hygiene measures or periodontal surgeries over the last 6 months at the area of interest

Design outcomes

Primary

MeasureTime frame
2. Clinical measurement: distance from the contact point (CP) to papillary tip using the prepared stent 3. Photographic measurement: 4. Radiographic measurement. The following distances will be measured a. Distance from CP to crest of the bone (BC) b. Interdental width at the level of facial CEJ Timepoint: follow up at 15th day, 1, 2, 3,4,5,6 months and the clinical and photographic parameters will be re-recorded

Secondary

MeasureTime frame
1. A questionnaire for assessment of patientâ??s response including questions regarding patientâ??s assessment of black triangleTimepoint: First day of treatment and after 6 months

Countries

India

Contacts

Public ContactDr Manish Khatri

Institute of Dental Studies and Technologies

komal_arora09@yahoo.co.in9818190603

Outcome results

None listed

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