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Comparative Evaluation of Melatonin Versus MTA on Vital Pulp Therapy in Young Permanent First Molars: An in Vivo Study

S

Suez Canal University

Status

Enrolling

Conditions

Dental Caries in Children
Vital Pulp Therapy

Treatments

Drug: Melatonin (dressing material)
Drug: Mineral trioxide aggregate (dressing material)

Study type

Interventional

Funder types

Other

Identifiers

NCT06372561
Melatonin- vital pulp therapy

Details and patient eligibility

About

The process of dental caries is dynamic and can be either reversible or irreversible depending on the balance between protective and pathologic factors in the oral cavity. Untreated dental caries causes pulpal injury, inflammation, and necrosis. Melatonin plays an essential role in the regulation of bone growth. The actions that melatonin exerts on odontoblasts may be similar to its action on osteoblasts.

Full description

The aim of this study is to evaluate and compare the pulp response of young permanent first molars after apexogenesis procedure, using melatonin versus MTA clinically and radiographically. This study will be performed on 45 young permanent first molars that will be divided equally into three groups according to the material used following apexogenesis; GroupI: MTA, GroupII: Melatonin and GroupIII: MTA and Melatonin. apexogenesis procedures will be carried out in children aged 6 to 8 years old. This will be followed by placement of MTA or/and Melatonin material as a sub base in the pulp chamber according to the group. Then, placement of a conventional glass ionomer cement (FUGI IX) as a permanent restoration will be conducted. Then, an immediate postoperative periapical digital x-ray film will be taken for the patients. The patient follow-up will be assigned 1,3,6,9 and 12 months after treatment.

Enrollment

45 estimated patients

Sex

All

Ages

6 to 8 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 1- Apparently healthy and medically free children. 2- Their age ranges from 6-8 years. 3- Both boys and girls will be included. 4- Children should have mandibular permanent first molars with the following clinical and radiographic criteria. 4.1Restorable young permanent first molars. 4.2Absence of clinical evidence of pulp degeneration:
  • No history of spontaneous pain, history of night pain or pain that not relieved by analgesics.
  • No pain on percussion.
  • No mobility.
  • Absence of abscess, purulent sinus or soft tissue edema.
  • Bleeding should stop within 5 minutes after the amputated pulp stumps.

Exclusion criteria

  • Internal root resorption.
  • External root resorption.
  • Inter radicular or periapical bone destruction (radiolucency)
  • A deep carious lesion radiologically that approaches the pulp

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

45 participants in 3 patient groups

Mineral Trioxide Aggregate
Active Comparator group
Description:
is a powder that consist of Calcium oxide, silicone dioxide, aluminum oxide, bismuth oxide, purified water. It is a bactericidal dressing material, promotes pulp healing, and does so without producing inflammation and promotes dentin bridge formation.
Treatment:
Drug: Mineral trioxide aggregate (dressing material)
Melatonin
Experimental group
Description:
(N-acetyl-5-methoxy-tryptamine) is a pleiotropic hormone synthesized in the pineal gland that has important chronobiotic properties. there is a Melatonin drug (powder) that proved to play an essential role in the regulation of bone growth (bone regeneration) and it may promote osteoblast differentiation, and stimulates mineralized matrix formation
Treatment:
Drug: Melatonin (dressing material)
Mineral Trioxide and Melatonin
Experimental group
Description:
Mixture of the two materials' powders.
Treatment:
Drug: Mineral trioxide aggregate (dressing material)
Drug: Melatonin (dressing material)

Trial contacts and locations

1

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Central trial contact

Mennatallah Hesham El shaabany, doctorate student; Asmaa Ali Abo El-Soud, Associate professor

Data sourced from clinicaltrials.gov

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