Clinical Performance of Low Technique Sensitive Self Cured Universal

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05211908` - Clinical Performance of Different Adhesive Strategies With a Universal System in Sclerosed Dentin in NCCL: A Double-blind Randomized Clinical Trial.	N/A
Completed	`NCT05635981` - Effect of an Additional Hydrophobic Adhesive Layer Application on the Class V Composite Restorations	N/A
Completed	`NCT04756349` - Clinical Performance of Adhesive Systems Containing HEMA and 10-MDP in Non Carious Cervical Lesions	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT05211908 - Clinical Performance of Different Adhesive Strategies With a Universal System in Sclerosed Dentin in NCCL: A Double-blind Randomized Clinical Trial.

N/A

Completed

NCT05635981 - Effect of an Additional Hydrophobic Adhesive Layer Application on the Class V Composite Restorations

N/A

Completed

NCT04756349 - Clinical Performance of Adhesive Systems Containing HEMA and 10-MDP in Non Carious Cervical Lesions

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04572386
Study type	Interventional
Source	Cairo University
Contact	Aya Gamal, masters
Phone	01004222615
Email	yoyo_ga@hotmail.com
Status	Not yet recruiting
Phase	N/A
Start date	October 2020
Completion date	July 2022

Clinical Performance of Low Technique Sensitive Self Cured Universal Adhesive Vrs Light Cured Universal Adhesive in Patients With (NCCLs): 18 m RCT

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms