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Effects of Rebonding Technique and Final Cure in Post-operative Hypersensitivity in Class 1 Composite Restorations

Effects of Rebonding Technique and Final Cure on Post-Operative Hypersensitivity in Class 1 Composite Restorations

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07041424
Enrollment
120
Registered
2025-06-27
Start date
2025-05-01
Completion date
2025-10-30
Last updated
2025-06-27

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

Conditions

Post-Operative Hypersensitivity

Keywords

Rebonding Technique, Post-Operative Hypersensitivity, Composite Restorations

Brief summary

Rebonding technique has been suggested to address the issue of post-operative hypersensitivity in composite restorations. it involves the application of bonding agent on composite restoration following finishing and polishing.

Detailed description

Rebonding technique has been suggested to address the issue of post-operative hypersensitivity in composite restorations. it involves the application of bonding agent on composite restoration following finishing and polishing. bonding agent fills the gap formed by polymerization shrinkage and hence prevent post-operative hypersensitivity

Interventions

PROCEDUREtreatment group 1: total etch bonding agent used with rebonding technique

class 1 composite restoration is done using total etch type bonding agent and rebonding technique applied

PROCEDUREtreatment group 2: self etch bonding agent used with rebonding technique

class 1 composite restoration is done using self etch type bonding agent and rebonding technique applied

Sponsors

Foundation University Islamabad
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

four groups. 2 control groups and 2 treatment groups. In group 1, total etch type bonding agent used but no rebonding done. In group 2, total etch bonding agent used and rebonding technique carried out. In group 3, self etch type bonding agent used but no rebonding done. in group 4, self etch bonding agent used and rebonding technique carried out.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* class 1 carious lesion in premolar and molars clinically diagnosed as moderate occlusal caries extending up to middle third of dentin no caries on any other surface of tooth patients with sign and symptom of reversible pulpitis like sharp pain, sensitivity to hot and cold and sweet stimuli lasting foe few seconds

Exclusion criteria

* history of generalized sensitivity cavities extending up to pulpal third of dentin cavities need to be restored with direct or indirect pulp capping poor oral hygiene or periodontal disease bruxism and other wear facets chronic anti inflammatory, analgesics or psychotropic drugs

Design outcomes

Primary

MeasureTime frameDescription
Post-operative hypersensitivityfrom treatment to 24 hours and 1 weekNumeric pain intensity scale 0= no sensitivity 1-3= mild sensitivity 4-6= moderate sensitivity 10=worst possible sensitivity

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026