Prospective Comparison of Indirect Pulp Therapy & Mineral Trioxide

See also
Status	Clinical Trial	Phase
Completed	`NCT06402032` - Clinical and Histological Evaluation of Hesperidin as a Direct Pulp Capping Material	N/A
Completed	`NCT02891876` - 3-months Success Rate of Direct Pulp Capping With Biodentine®	N/A
Active, not recruiting	`NCT03403985` - Long-term Evaluation of Direct Pulp Capping	N/A
Completed	`NCT03606681` - Clinical and Radiographic Evaluation of Indirect Pulp Capping in Primary and Permanent Teeth With Different Materials	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT06402032 - Clinical and Histological Evaluation of Hesperidin as a Direct Pulp Capping Material

N/A

Completed

NCT02891876 - 3-months Success Rate of Direct Pulp Capping With Biodentine®

N/A

Active, not recruiting

NCT03403985 - Long-term Evaluation of Direct Pulp Capping

N/A

Completed

NCT03606681 - Clinical and Radiographic Evaluation of Indirect Pulp Capping in Primary and Permanent Teeth With Different Materials

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	NCT02620826
Study type	Interventional
Source	University of Michigan
Contact
Status	Completed
Phase	N/A
Start date	December 2013
Completion date	December 2019

Prospective Comparison of Indirect Pulp Therapy and Mineral Trioxide Aggregate Pulpotomy in Decayed Primary Molars

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms