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A study to determine if the process of warming composite resin restorative material prior to placement of a restoration leads to any changes in post operative sensitivity

A study to determine if the process of warming composite resin restorative material prior to placement of a restoration leads to any changes in post operative sensitivity: a parallel sided randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN76727312
Enrollment
120
Registered
2013-03-19
Start date
2013-01-08
Completion date
Unknown
Last updated
2019-02-11

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

Conditions

Restorative dentistry Oral Health Restorative dentistry

Interventions

The interventions are the routine placement of composite restorative material in a prepared tooth cavity (a dental ?filling?). For the control this is with the filling material at room temperature (i.

Sponsors

University of Leeds (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patient is over 18 2. Patient is under 70 3. Either sex 3. Patient is capable of informed consent 4. The tooth responds to sensitivity testing (?vitality test? with an electric pulp tester) 5. The cavity to be restored is a one or two surface cavity 6. The cavity is suitable for composite restoration and the patient prefers composite to amalgam

Exclusion criteria

Exclusion criteria: 1. The tooth does not respond to an electric pulp test 2. The patient is incapable of giving informed consent 3. The patient is a child under 18 4. The patient is unable to return the Visual Analogue Scale (VAS) assessment sheets at the appropriate time 5. The tooth to be filled is periodontally involved (grade 2 or grade 3 mobile) 6. The tooth to be filled is an abutment tooth for a removable prosthesis 7. The tooth to be filled has undergone orthodontic treatment within the last 3 months 8. The tooth to be filled has had periodontal surgery within the last 3 months

Design outcomes

Primary

MeasureTime frame
VAS assessment 24 hours after treatment

Secondary

MeasureTime frame
VAS assessment 7 days, 14 days and 1 month after treatment

Countries

United Kingdom

Outcome results

None listed

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