Skip to content

The Comparison of Acellular Dermal Matrix Allograft (CenoDerm) and a Subepithelial Connective Tissue Graft for the Treatment of Gingival Recession.

The Comparison of Acellular Dermal Matrix Allograft (CenoDerm) and a Subepithelial Connective Tissue Graft for the Treatment of Gingival Recession.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT201305201760N23
Enrollment
24
Registered
2013-08-23
Start date
2013-05-22
Completion date
Unknown
Last updated
2018-02-22

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: Transport Coronal flap with connective tissue graft placement method is treated [CPF(coronally positioned flap ) + CTG(Connective Tissue Graft )]. Intervention 2: Inter
Treatment - Surgery
Control group: Transport Coronal flap with connective tissue graft placement method is treated [CPF(coronally positioned flap ) + CTG(Connective Tissue Graft )]
Intervention group: With Acellular dermal matrix allograft (CenoDerm) (manufactured by replicating tissues Creed) and coronal displacement of the flap can be treated. [ADMA(Acellular Dermal Matrix A

Sponsors

Vice Chancellor for Research and Technology, Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Analysis of single-sided facial tissue depth of 2mm = X CEJ in teeth or premolars; All sub-group analyzes of Miller class I / II; Selected teeth without fillings and no bleeding after probing; Persons 18 years and older; Ability to maintain good oral hygiene (% 20 O'Leary plaque score =); Vestibule depth of enough. Exclusion criteria: Pregnancy; use of drugs interfering with wound healing (corticosteroids, anti-cancer), or medicines that may cause gingival enlargement; Smoking; which prohibits any local or systemic disease, periodontal surgery is prescribed; Traumatic brushing methods; Hard toothbrushes or toothpaste abrasives; History of periodontal surgery in the past 2 years; The use of removable prosthodontic or orthodontic appliances in the area.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Treatment of Gingival Recession. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical photography.

Secondary

MeasureTime frame
Discomfort after surgery. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Indexed pain (VAS).;Vertical recession depth (VRD). Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical (in mm).;Healing. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Landry Index.;Cosmetic results. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Aesthetic Index (VAS).;Clinical attachment level. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical (in mm).;Probing depth. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical (in mm).;Gingival thickness. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical (in mm).;Mgj distance to CEJ. Timepoint: 1 month, 3 months, 6 months after surgery. Method of measurement: Clinical (in mm).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Masoomeh Haghpanah Aski

Dental College of Babol

parya_haghpanah@yahoo.com+98 11 1229 1408

Outcome results

None listed

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