a clinical trial to compare the effect of a tooth-colored filling material directly filled in the damaged area of the tooth with a tooth-colored filling material which is heated and then applied to the damaged area.

A one-year comparative clinical evaluation of direct composite with direct-indirect heat tempered composite restoration technique in non-carious cervical lesions. -A split mouth randomized clinical study. - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/054535

Enrollment

Registered

2023-06-28

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Health Condition 1: K031- Abrasion of teeth

Interventions

Intervention1: Direct-indirect heat tempered composite restoration technique: Direct-indirect heat tempered composite restoration technique in restoration of non-carious cervical lesions Control Inter

Eligibility

Inclusion criteria

Inclusion criteria: Systemically healthy patients aged between 18-65 years with a minimum of 1 mm deep lesion on the buccal surface of anterior teeth and premolars involving both sides of the arch will be enrolled for the study. Patients with good oral hygiene and with opposing teeth in contact will be included. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria: Teeth with caries, pulpal and/ or periapical pathology, severe periodontal disease, developmental anomaly, or congenital defects will be excluded. Deep cervical abrasions with exposed pulp. Teeth that had received endodontic treatment will be excluded. Patients with malocclusion rotated teeth or undergoing orthodontic treatment along with any parafunctional habits will be excluded. Teeth that have to be used as an abutment will be excluded. Pregnant and lactating women will be excluded.

Design outcomes

Primary

Measure	Time frame
To compare the clinical performance of direct-indirect with direct composite restoration technique in Non-Carious Cervical lesions Timepoint: Baseline, 6 months, 12 months	—

Secondary

Measure	Time frame
To evaluate the clinical performance of direct indirect composite restoration technique in non-Carious cervical lesions Timepoint: Baseline, 6 months, 12 months	—

Countries

India

Contacts

Public ContactDr Nimisha Shah

Km Shah Dental College and Hospital

nshah7873@gmail.com9998994299

Outcome results

None listed

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