Reversible Pulpitis Clinical Trial
Official title:
Role Of Wound Lavage in Direct Pulp Capping Of Permanent Teeth With Carious Exposure: A Randomized Controlled Trial
Verified date | May 2023 |
Source | Postgraduate Institute of Dental Sciences Rohtak |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
the purpose of the study is to investigate the outcome of wound lavage agents Sodium hypochlorite and Ethylenediaminetetraacetic acid (EDTA) in direct pulp capping of mature permanent teeth with carious exposure.
Status | Active, not recruiting |
Enrollment | 140 |
Est. completion date | May 31, 2024 |
Est. primary completion date | April 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: 1. Patient willing to participate in the study. 2. Age group- 18-50 years. 3. Mature permanent mandibular posterior teeth (molars or premolars) with reversible pulpitis. 4. Teeth with extremely deep caries (Caries penetrating entire thickness of dentine) responding within normal limits to the cold test and Electric pulp test. 5. Teeth with normal apical tissues(not showing any rarefaction on the intraoral periapical radiograph) Exclusion Criteria: 1. Primary teeth. 2. Teeth with irreversible pulpitis (spontaneous pain) or pulp necrosis, chronic periodontitis, cracked tooth, internal or external resorption, calcified canals, associated with sinus tract, and furcation or apical radiolucency. 3. Immuno-compromised, diabetic, pregnant and hypertensive patients. 4. Positive history of antibiotic within past one month and analgesic since one week use of the treatment |
Country | Name | City | State |
---|---|---|---|
India | PGIDS | Rohtak | Haryana |
Lead Sponsor | Collaborator |
---|---|
Postgraduate Institute of Dental Sciences Rohtak |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | clinical and radiographic success at 6 and 12 months. | Clinical success criteria-
Positive response on cold testing Absence of sign and symptoms of spontaneous pain or pain on stimulus and discomfort. No tenderness to palpation or percussion and the tooth is functional. Normal tooth mobility and no periodontal probing pocket depth. Soft tissues around tooth are normal with no swelling or sinus tract. Radiographic success criteria- Absence of any periapical or interradicular radiolucency Absence of internal or external root resorption Periapical Index score < 2 according to Orstavik et al. |
12 months | |
Secondary | To assess postoperative pain . | To assess incidence and intensity of pain postoperatively at every 24 hours till 7 days using Visual analogue Scale of 0 to 10 centimeter line. Score 0 means no pain and Score 10 means maximum pain | 7 days |
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