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Determining the effectiveness of various gingival retraction techniques included cord,paste,laser

Determining the effectiveness of various gingival retraction techniques included cord,paste,laser on the periodontal indicators ,after impression in fixed prosthesis:a randomized clinical trial study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160213026538N6
Enrollment
60
Registered
2021-01-07
Start date
2021-01-02
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Gingival retraction

Interventions

Intervention 1: Intervention group: retraction gingiva with paste. Intervention 2: Intervention group: retraction gingiva with laser. Intervention 3: Intervention group: retraction gingiva with cord.

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients who need their maxillary or mandibular first molar to be restored have the opposite teeth in functional occlusion and at least one proximal contact with the adjacent teeth have clinical sulcus depth between 2-3 mm and thick gingiva biotype dont be a smoker Acceptable oral hygiene and periodontally healthy(plaque index and bleeding on probing had to be below 20% previously to the prosthodontic treatment) ready to take part in the study and sign the testimonial

Exclusion criteria

Exclusion criteria: have previous periodontal surgery have mobility in tooth use drugs having effect on periodontium patients have systemic disease

Design outcomes

Primary

MeasureTime frame
Recession. Timepoint: after one and two week. Method of measurement: scanned reference on first session.;Gingival index. Timepoint: at the first session, after one and two week. Method of measurement: gingival index.;Plaque index. Timepoint: at the first session, after one and two week. Method of measurement: plaque index.;Bleeding index. Timepoint: at the first session, after one and two week. Method of measurement: bleeding index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Naeemi

Kermanshah University of Medical Sciences

alinaeemi420@yahoo.com+98 83 3727 7030

Outcome results

None listed

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