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examining the effects of different rubber dam sealing materials

Not Applicable
Registration Number
CTRI/2022/02/040536
Lead Sponsor
Dr Jaimini Patel
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Systemically Healthy individuals,i.e., class I patients according to American society of anesthesiology(ASA) classification 12 between the age group of 18 to 65 years with a leaking rubber dam in the mandibular arch will be included for the study.

2.Patients with partially erupted, maligned, compromised teeth which need endodontic procedures or deep marginal elevation will be included.

3.Patients requiring gingival protection when performing porcelain repair, cementation of veneers, vital bleaching, all ceramic crowns, inlay, onlay in the mandibular arch will be included in this study.

4.A written informed consent will be taken from all the patients and only those patients who are ready to sign the consent form will be included in the study.

Exclusion Criteria

1.Patients with poor oral hygiene will be excluded from the study.

2.Patients with severe or chronic periodontitis with gingival recession will be excluded.

3.Patients with latex allergy will be excluded.

4.Teeth with a maxillary arch will not be included in the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the efficacy of liquid dam,kooldam and oraseal cauking rubber dam sealing materials used during isolation procedures.Timepoint: at baseline
Secondary Outcome Measures
NameTimeMethod
Clinical evaluation of sealing ability,seepage,ease of adaptability and removal of dam seal material after 30 mins of procedure.Timepoint: baseline
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