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The comparison of Papilla preservation technique and pouch& tunnel with subepithelial connective tissue graft in dark triangle treatment

The comparison of Papilla preservation technique and pouch& tunnel with subepithelial connective tissue graft in dark triangle treatment

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201404071760N34
Enrollment
10
Registered
2014-05-04
Start date
2014-03-11
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: Intervention group 1: The first incision is semilunar 3 mm below MGJ .The second incision is sulcular .In semilunar incision flap is reflected full thickness .SCTG is taken from t
Treatment - Surgery
Intervention group 1: The first incision is semilunar 3 mm below MGJ .The second incision is sulcular .In semilunar incision flap is reflected full thickness .SCTG is taken from the palate in pr
Intervention group 2: Papilla preservation technique :papilla preservation incision is used and in cases where the width of papilla is short for better vascularization the horizontal incision is

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: existence the dark triangle anterior max; Tarnow all black triangles classified under group I, II; the selected teeth vital and no bleeding after probing; people over 18 years old; ability to maintain good oral hygiene (Oleary plaque score <20%); without stretching the frenum Exclusion criteria: pregnancy; history of blood clotting problems, and hematologic; interfere with the healing agents (corticosteroids, anticancer); drugs interfering with platelet function (NSAIDS); smoking; any local or systemic disease with surgical procedures to prohibit administration; traumatic methods of brushing, toothbrush, toothpaste abrasives or harsh; long-term use of antibiotics in the previous quarter (more than 2 weeks); with known allergies to materials used in surgery; active infectious diseases (tuberculosis, hepatitis, HIV); use of drugs can lead to gingival enlargement.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Treatment of dark Triangle. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Indexed Nordland and Tarnow.

Secondary

MeasureTime frame
APico - coronal Papilla dimension. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Mm.;MOD Papilla dimension. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Mm.;Healing. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Healing index.;Beauty. Timepoint: Before surgery and three and six months after surgery. Method of measurement: Indexed beauty VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Morteza Rahimi Rad

Dental colleges of Babol

mortezadds@yahoo.com+98 11 1229 1408

Outcome results

None listed

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