Analgesic Effect of Anahil and Ibuprofen on Pain After Root Canal Therapy in Patients With Pulpitis of the Molars in Qazvin(a City in Iran)

NCT ID: NCT05349929

Last Updated: 2022-04-27

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 72 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-31
• Study Completion Date: 2022-12-31

Brief Summary

Hypothesis:

0: The analgesic effect of Ibuprofen and Anahil would be the same in reducing the pain after root canal therapy.

1: Ibuprofen shows higher potency to reduce the pain after root canal therapy.

1: Anahil shows higher potency to reduce the pain after root canal therapy.

1. combination of the Anahil and Ibuprofen would have more effective results in reducing the pain post endodontic treatment.

Detailed Description

Patients will be selected from those who are referred to receive root canal therapy for the mandibular first molars with irreversible pulpitis.

The current research and all the procedures will be done in a private dental clinic in Qazvin, Iran by a single endodontist.

72 Patients who will meet our study demands and criteria would be qualified to enter the study and will sign the informed consent form explaining the study circumstances and its possible risks.

Patient information sheet includes dental, medical and drug history and demographic information will be obtained as well. Radiographic examination includes the amount of caries, root curvature, periapical and hard tissue situation, dental pulp vitality tests including Electrical Pulp Test(EPT) and thermal tests (heat and cold) and periapical tests consisting of percussion and palpation would be recorded. The patients would be divided randomly in Ibuprofen and Anahil groups, these drugs would be put in the same shape and appearance by a pharmacist and named as A and B respectively. Anahil capsules containing 200 mg of bromelain, Permon-Amin Health Company, Gelofen 400mg capsules, Dana-Pharma company:The pre procedure pain of the patients would be asked and recorded by Visual Analogue Scale(VAS), a 100 mm long ruler which has no numeration by means of enhancing the accuracy and minimizing the failure. Standard Infra alveolar nerve(IAN) direct block will be done by injection of 1.8ml of lidocaine 2% containing 1:100000 epinephrine with a long 32mm gauge 27 needle. The efficiency of Inferior Alveolar Nerve block injection will be examined with the numbness of inferior lip. Supplementary anesthesia (like intrapulpal or Periodontal Ligament(PDL) anesthesia) will be used if the pain is still remained after 15 minutes. After tooth isolation with rubberdam, caries removal, access cavity and tooth preparation will be done. Length determination will be performed with the help of periapical radiography and apex locator. Cleaning and shaping will be done. Normal Saline and hypochlorite 2% will be used as intracanal irrigants. The canals will then be dried and gutted laterally with gutta-percha and AH+ sealer. A cotton pellet will be placed in the access cavity. Temporary restoration will be applied after occlusal reduction and the occlusion will be checked. No intracanal medicament will be placed. In this triple blinded study, patients will be given A and B drugs (36 patients in each group, equal in gender) with medications order randomly and will be followed 6, 12, 24 and 48 hours after endodontics treatment to report the pain score with VAS and the number of supplementary dosage of Ibuprofen with the time that they have consumed.

Conditions

Irreversible Pulpitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Ibuprofen

Ibuprofen(Gelofen) 400mg capsules, Dana pharma company, every 6hours

Group Type: EXPERIMENTAL

Gelofen (generic name of Ibuprofen in Iran)

Intervention Type: DRUG

Gelofen capsules, 400mg Ibuprofen, Dana pharma company, every 6hours

Root Canal Therapy

Intervention Type: PROCEDURE

all the participants go under RCT.

Anahil

Bromelain(Anahil) 200 mg capsules, Permon Amin Health Company,every 6hours

Group Type: EXPERIMENTAL

Anahil ( generic name of Bromelain in Iran)

Intervention Type: DRUG

Anahil capsules,200 mg Bromelain, Permon Amin Health Company,every 6hours

Root Canal Therapy

Intervention Type: PROCEDURE

all the participants go under RCT.

Interventions

Gelofen (generic name of Ibuprofen in Iran)

Gelofen capsules, 400mg Ibuprofen, Dana pharma company, every 6hours

Intervention Type: DRUG

Anahil ( generic name of Bromelain in Iran)

Anahil capsules,200 mg Bromelain, Permon Amin Health Company,every 6hours

Intervention Type: DRUG

Root Canal Therapy

all the participants go under RCT.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Patients report spontaneous pain of the first molar of mandible ranging from 50 to 100 mm on a VAS (0-100 mm)

2. The dental pulp's condition is irreversible pulpitis and the tooth is reparable and need the root canal therapy

3. No evidences of any lesions and lucency, PDL widening, loss of lamina dura in radiographic examination

4. Patients aged 20 to 50 years from both genders

5. Patients are not pregnant or breast-feeding

6. Healthy periodontal status (no evidences of aggressive/chronic periodontal diseases)

7. No history of any systemic diseases (specially gastrointestinal and coagulation disorders)

8. No history of allergic reaction to food nutrients (specially pineapple, celery, carrot, and fennel), NSAIDs and lidocaine

9. No history of consuming the drugs interfere with NSAIDs, lidocaine and anticoagulants

10. No use of other analgesic drugs within the last 6 hours

11. Existence of no large restorations or crowns in treated tooth

12. patients have no extreme fear of dental procedure

13. Teeth with no evidence of infection or sinus tract

14. Patients did not a previous RCT

Exclusion Criteria

1. Patients who leave the study because of any reasons

2. Special anatomy of teeth (extra canals, severe root curvature, calcifications, open apex, C shape, fractures,..)

3. Patients who are not able to tolerate the single-session treatment (time, tooth's situation,..)

4. If the aspiration through IAN block injection is positive

5. If the diagnosis of pulp status has changed to partial necrosis during access cavity preparation

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Qazvin University Of Medical Sciences

OTHER

Sponsor Role: lead

Responsible Party

Mona Esfahani

Dentistry Student

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Mahsa Esfehani, Ms

Role: STUDY_DIRECTOR

associate professor of oral medicine of Qazvin University Of Medical Sciences

Central Contacts

Mona Esfahani, Student

Role: CONTACT

monaes2424@gmail.com

+989120407509

Other Identifiers

1111

Identifier Type: -

Identifier Source: org_study_id