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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05681494
Other study ID # 28/12/2022
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date February 26, 2023
Est. completion date June 26, 2024

Study information

Verified date February 2023
Source Cairo University
Contact Amany IA mohamed, phd
Phone 01099300346
Email amany.ahmed@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assessment of postoperative pain and treatment success after vital pulp therapy versus root canal treatment in mandibular molar with signs and symptoms of irreversible pulpitis. the null hypothesis, there is no difference will be observed in the pain level and treatment success between two treatments.


Description:

After proper clinical and radiographic examination. Teeth will be anesthetized and isolated using a rubber dam. The operative field will be disinfected. Total caries removal will be done from outside making margin caries free to inside. the new diamond bur will be used to remove the last layer and exposed the pulp tissue. Exposed pulp will be inspected under a dental operating microscope and hemostasis will be obtained. The teeth will be randomized into 2 intervention groups (VPT or RCT). Treatment will be finalized, and teeth will be restored with resin-modified glass ionomer followed by composite resin at the same appointment. Ibuprofen 400mg will be prescribed to the patient if needed. Patients will be asked to record postoperative pain after treatment on the pain score sheet.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 44
Est. completion date June 26, 2024
Est. primary completion date July 26, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Systemically healthy patients. - Patient's age range more than 15 years. - Mature permanent mandibular molars with deep caries. - Clinical diagnosis of symptomatic irreversible pulpitis. - Teeth with no need for the post. - Healthy periodontium and mobility within normal limits. - Patients who can understand the pain scale and can sign the informed consent Exclusion Criteria: - Teeth with a negative response to vitality testing. - Teeth with furcal bone loss. - Teeth with sinus tract - Teeth with swelling. - Teeth with a non-restorable crown. - Teeth with immature roots. - Teeth with no pulp exposure even after caries excavation. - History of analgesic intake in the previous week. - History of antibiotic intake in the previous month. - Insufficient bleeding after pulp exposure suggestive of partial necrosis of the pulp. - Inability to control bleeding within 10 min. - Radiographic evidence of external or internal root resorption vertical root fracture, perforation, calcification.

Study Design


Related Conditions & MeSH terms

  • Pulpitis
  • Symptomatic Irreversible Pulpitis

Intervention

Procedure:
Root canal treatment
after access cavity preparation, the working length will be determined. chemo-mechanical preparation will be done, and teeth will be obturated. final restoration will be placed.
Vital pulp therapy
exposed pulp will be capped with 3 mm calcium silicate material

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

References & Publications (4)

Asgary S, Eghbal MJ, Shahravan A, Saberi E, Baghban AA, Parhizkar A. Outcomes of root canal therapy or full pulpotomy using two endodontic biomaterials in mature permanent teeth: a randomized controlled trial. Clin Oral Investig. 2022 Mar;26(3):3287-3297. doi: 10.1007/s00784-021-04310-y. Epub 2021 Dec 2. — View Citation

Santos JM, Pereira JF, Marques A, Sequeira DB, Friedman S. Vital Pulp Therapy in Permanent Mature Posterior Teeth with Symptomatic Irreversible Pulpitis: A Systematic Review of Treatment Outcomes. Medicina (Kaunas). 2021 Jun 3;57(6):573. doi: 10.3390/medicina57060573. — View Citation

Taha NA, Al-Khatib H. 4-Year Follow-up of Full Pulpotomy in Symptomatic Mature Permanent Teeth with Carious Pulp Exposure Using a Stainproof Calcium Silicate-based Material. J Endod. 2022 Jan;48(1):87-95. doi: 10.1016/j.joen.2021.09.008. Epub 2021 Sep 24. — View Citation

Taha NA, Al-Rawash MH, Imran ZA. Outcome of full pulpotomy in mature permanent molars using 3 calcium silicate-based materials: A parallel, double blind, randomized controlled trial. Int Endod J. 2022 May;55(5):416-429. doi: 10.1111/iej.13707. Epub 2022 Mar 17. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pain postoperative pain will be recorded by patient using NRS at 6 hours postoperative
Secondary Intensity of postoperative pain postoperative pain will be recorded by patient using NRS at 24, 48 hours and 7 days
Secondary Treatment success clinical and radiographic success at 3,6,12 months
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