3D Instrumentation Versus Rotary Instrumentation

Postoperative Pain Clinical Trial

Official title:

The Effect of 3D Instrumentation Versus Rotary Instrumentation on Postoperative Pain and Bacterial Reduction in Necrotic Oval Canals: A Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03285334
• Other study ID #: CEBD-CU-2017-09-19
• Status: Not yet recruiting
• Phase: N/A
• First received: September 13, 2017
• Last updated: September 14, 2017
• Start date: November 2017
• Est. completion date: November 2018

Study information

• Verified date: September 2017
• Source: Cairo University
• Contact: radwa emara
• Phone: 01272141312
• Email: radwa.emara[@]dentistry.cu.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

enrollment of the patient after diagnosis, radiographic evaluation, and signing the informed consent.

allocation of the patient to either intervention or control group. After anaesthesia and access cavity, the first root canal sample will be taken. Endodontic treatment will be completed in one visit. The second root canal sample will be taken. Patients will be asked to evaluate their postoperative pain level using VAS scale at 6, 12, 24 hours, and daily up to 5 days. Patients will record the number of analgesics if any taken.

Description:

After diagnosing the case as asymptomatic pulp necrosis and confirming that the patient conforms to all eligibility criteria, (R.S) will enroll the patient in the study.

the operator will complete treatment of all cases in single visit as following:

1. Anesthetizing the tooth using inferior alveolar nerve block technique

2. Removal of Caries and/or coronal restorations completely with sterile bur and rubber dam will be applied.

3. Preparation of access cavity using another sterile round carbide bur size 3 and Endo-z bur .

4. (R.S) will take the preinstrumentation root canal sample (S1)

5. Confirming the patency of the root canals using stainless steel hand K-files size #10 and #15 . Working length will be determined .

6. In the intervention group, (R.S) will perform mechanical preparation in a 3D manner using Xp-endo Shaper single file in an endodontic motor at a speed of 800 rpm and a torque of 1 Ncm.

7. In the control group, mechanical preparation will be done using rotary iRace files (#25/0.04, #30/0.04, and #40/0.04) at a speed of 600 rpm and a torque of 1.5 Ncm. The canal will be irrigated and recapitulated after the use of each instrument.

8. EDTA gel will be used as a lubricant. The canals will be thoroughly irrigated using 3ml of 2.5% sodium hypochlorite.

9. The canal will then be dried by using sterile paper points and then flushed with 5 ml of 5% sodium thiosulfate to inactivate the NaOCl. The postinstrumentation sample (S2) will be taken from the canals.

10. Master cones will be fitted to the working length and a radiograph will be taken to ensure proper length.

11. (R.S) will complete obturation using AdSeal resin-based root canal sealer .

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 50
• Est. completion date: November 2018
• Est. primary completion date: February 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Healthy Adult patients.

2. Age between 20-40 years old.

3. Males & Females.

4. Asymptomatic necrotic mandibular premolars with or without periapical radiolucency.

5. Normal occlusal contact with the opposing teeth.

6. Patients accepting to participate in the study.

Exclusion criteria:

1. Medically compromised patients

2. Pregnant women

3. If analgesics or antibiotics have been administrated by the patient during the past 12 hours preoperatively

4. Patients reporting bruxism or clenching

5. Teeth that shows:

• Association with acute periapical abscess and swelling

• Greater than grade I mobility or pocket depth greater than 5mm

• No restorability

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Device:
• XP-endo Shaper
mechanical preparation in a 3D manner using Xp-endo Shaper
• iRace files
rotary mechanical preparation

Locations

Country	Name	City	State
Egypt	Faculty of Oral and Dental Medicine - Cairo University	Cairo	Manial

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative Pain	Degree of postoperative pain will be measured by the patients using modified VAS	up to 5 days
Secondary	intracanal bacterial reduction	The intra-canal bacterial count will be determined using culture technique in the microbiological department, Cairo University. Samples in RTF vials will be dispersed with vortex for 30 seconds by the laboratory technician. The RTF solution will be serially diluted one-tenth dilution and spiral plated onto the agar medium. The plates will be incubated at 37?c aerobically and anaerobically.; The resultant anaerobic growth will be quantified by evaluating the colony forming units (CFU) on the agar medium under the microscope and the number of CFU per milliliter of each dilution will be calculated for each sample.	6 hours
Secondary	Incidence of analgesic intake	In case of presence of moderate or severe postoperative pain, (R.S) will instruct the patients to take only one capsule of placebo given to him/her at the end of the visit (Powdered milk packed in opaque capsules)	up to 5 days