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Compares treatment options for Comparison of Bulk Fill vs HVGIC in Class II Cavities
Official title Clinical Performance of HVGIC vs Bulk Fill Composite in Class II Cavities of Posterior Teeth: A 12-Month RCT
ClinicalTrials.gov ID: NCT07067164
What this study is testing
- What it's testing
- Study Title: Clinical Performance of Highly Viscous Glass Ionomer versus Bulk Fill Resin Composite Restorative Materials in Moderate Class II Cavities of Permanent Posterior Teeth: A 12-Month Randomized Clinical Study Study Design: Split-mouth, randomized clinical trial on 31 patients with at least two moderate Class II carious lesions in permanent posterior teeth. Each patient receives two restorations-bulk fill resin composite on one side and highly viscous glass ionomer (HVGIC) on the other.
- Time commitment: about 1 week
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45. Healthy volunteers may be eligible.
You may be able to join if
- Patients aged 18 to 45 years
- Systemically healthy individuals
- Patients with at least two Class II carious lesions (one on each side) in permanent posterior teeth
- Vital, symptomless teeth
- Teeth in occlusion and in contact with adjacent natural teeth
You likely can't join if
- Medically compromised patients
- Pregnant or breastfeeding women
- Poor oral hygiene
- Patients undergoing orthodontic treatment
- Patients with parafunctional habits (e.g., bruxism)
- Extensive lesions requiring cusp coverage
See the full eligibility criteria
- Patients aged 18 to 45 years
- Systemically healthy individuals
- Patients with at least two Class II carious lesions (one on each side) in permanent posterior teeth
- Vital, symptomless teeth
- Teeth in occlusion and in contact with adjacent natural teeth
- Healthy periodontal tissues
- Carious lesions of moderate depth (outer or middle third of dentin radiographically)
- Patients likely to return for recall visits
- Medically compromised patients
- Pregnant or breastfeeding women
- Poor oral hygiene
- Patients undergoing orthodontic treatment
- Patients with parafunctional habits (e.g., bruxism)
- Extensive lesions requiring cusp coverage
- Absence of adjacent or opposing teeth
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Cairo Governorate, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 1 week per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 45 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Cairo Governorate, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.