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Treatment of retracted gums using tissues which underline the roof of the mouth with two surgical scalpels

Connective tissue graft harvesting with double bladed scalpel and traditional scalpel for treatment of gingival recession. a comparative randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN34968827
Enrollment
10
Registered
2020-02-07
Start date
2020-02-06
Completion date
Unknown
Last updated
2021-09-20

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

Conditions

Gingival recession of Miller's class I Oral Health

Interventions

This study will compare between two scalpels to harvest a connective tissue graft for treatment of gingival recession. The first one will be used in (test group) is double bladed sca

Sponsors

Damascus University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age between 18 - 55 years 2. There is no systematic disease that affects the wound healing 3. Good oral hygiene with no symptoms of gingivitis 4. No smoking habit 5. Bilateral side of gingival recession ( Miller's class I ) 6. At least 1mm of attached gingiva.

Exclusion criteria

Exclusion criteria: 1. Systemic disease or medication that affects wound healing 2. Gingival or periodontal disease or uncontrolled plaque accumulation 3. Pregnancy and breast-feeding

Design outcomes

Primary

MeasureTime frame
Current primary outcome measure as of 09/09/2021: 1. Recession Depth (RD) is measured by a UNC15 periodontal probe from a stable point (acrylic splint made for each patient) to the gingival margin at two time points: date of surgery, and after three months 2. Keratinized Tissue Width (KTW) is measured by a UNC15 periodontal probe at two time points: date of surgery, and after three months Previous primary outcome measure: 1. Recession Depth (RD): is measured by a UNC15 periodontal probe from a stable point (acrylic splint made for each patient) to the gingival margin at two time points: date of surgery, and after three months 2. Gingival Width (GW) :is measured by a UNC15 periodontal probe at two time points: date of surgery, and after three months

Secondary

MeasureTime frame
Current secondary outcome measures as of 09/09/2021: 1. Gingival Thickness (GT) is measured by a UNC15 periodontal probe at two time points: date of surgery, and after three months 2. Clinical Attachement Level ( CAL) is measured by a UNC periodontal probe from a stable point (acrylic splint) to the bottom of the gingival sulcus at two time points: date of surgery, and after three months 3. Surgical procedure time measured from the beginning of the surgery to the end of suturing 4. Pain level after surgery measured using vascular analogue scale (VAS) after three months 5. Patient satisfaction with esthetic results after surgery measured using vascular analogue scale (VAS) after three months Previous secondary outcome measures: 1. Gingival Thickness (GT) : is measured by a UNC15 periodontal probe at two time points: date of surgery, and after three months 2. Clinical Attachement Level ( CAL) : is measured by a UNC periodontal probe from a stable point ( acrylic splint ) to the bottom of the gingival sulcus

Countries

Syria

Outcome results

None listed

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