Effect of Etidronate in Sodium Hypochlorite Versus Sodium Hypochlorite on the Intensity of Postoperative Pain

Cairo University (CU)

Status

Unknown

Conditions

Necrotic Pulp

Treatments

Combination Product: sodium hypochlorite

Combination Product: etidronate in sodium hypochlorite

Study type

Interventional

Funder types

Other

Identifiers

NCT04035330

ETID_NAOCL

Details and patient eligibility

About

To compare the effect of using Etidronate in sodium hypochlorite versus sodium hypochlorite irrigating solution on:

Postoperative pain in patients with necrotic pulp.
Bacterial load reduction & main bacterial species detected preinstrumentation and post-instrumentaion
Periapical Matrix metalloproteinase 9 level (MMP-9) postinstrumentation and pre-obturation

Full description

Patients will be clinically and radiographically examined and their eligibility will be assessed Eligible patients will be treated in 2 visits

Anesthetizing the tooth using inferior alveolar nerve block technique by local anesthesia of 1.8 ml of 2% Mepivacaine with 1:100,000 epinephrine.
Removal of caries and/or coronal restorations completely with sterile bur and rubber dam will be applied.
Cleaning the operative field, including the tooth, the clamp, and rubber dam sheet, with 30% hydrogen peroxide until no further bubbling of the peroxide occurred. All surfaces will then be disinfected by a sterile cotton swab with a 5.25% sodium hypochlorite solution.
Preparation of access cavity using another sterile round carbide bur size 3 and Endo-z bur.
After completing the access, the operative field and the pulp chamber will be cleaned and disinfected once again in the same way mentioned above. NaOCl will be then neutralized with 5% sodium thiosulfate.
The patients will be randomly divided into 2 groups. Intervention group (9% Etidronate in 2.5% sodium hypochlorite root canal irrigant /Dual rinse) and control group (2.5% sodium hypochlorite root canal irrigant).
Confirming the patency of the root canals using stainless steel hand K-files size #10 and #15. Working length will be determined using an electronic apex locator then confirmed radiographically to be 1 mm shorter than radiographic apex. The canals to be enlarged to size #20.
The pre-instrumentation root canal sample (S1) as follows: a sterile paper point will be placed in the wider /largest canal to soak up the fluid in the canal with saline to a level approximately 1 mm short of the tooth apex based on diagnostic radiographs and estimated working length. The paper point will be left in the canal for at least 1 minute. Paper points will then be transferred aseptically to tubes containing 20 ml of sterile thioglycollate broth.
Mechanical preparation will be done using M PRO rotary files in an endodontic motor.The first file (18/.09) will be used as an orifice opener for two thirds of the working length followed by (20/.04) for the full working length and finally (25/.06). In-and-out motions will be applied with stroke lengths not exceeding 3 mm in the cervical, middle, and apical thirds until attaining the established working length. The first file is used with a continuous rotary motion at a speed of 500 rpm and torque of 3 Ncm. The second and third files are both used with a speed of 500 rpm and torque of 1.5 Ncm. The canal will be irrigated and recapitulated after the use of each instrument.
The canals will be thoroughly irrigated with the allocated irrigant (5ml for 1 min) using plastic disposable syringe with needle gauge 30 reaching 1 mm short of the working length. All teeth will receive the same volume of irrigant (25 ml)
The canal will then be dried by using sterile paper points and then flushed with 5 ml of 5% sodium thiosulfate followed by 5 ml distilled water to inactivate the NaOCl. The postinstrumentation sample (S2) will be taken from the canal as described above. In addition, the periapical sample (S3) will be collected after cleaning and shaping by introducing a fine sterile size 20 paper point 2 mm beyond the canal terminus for 1 min. This procedure was performed twice. The paper points were placed in a sterile micro-centrifugation tube (Merck) containing 2 mL of sterile physiological saline solution, and immediately transferred to a -80 °C freezer until further processing.
The access cavities will be closed using sterile cotton pellet and temporary filling and patients will be recalled after 1 week.
The patients will record their pain level on Visual analogue scale & Numerical rating scale at 6,12, 24 and 48 hours.
In the recall appointment after 1 week. Rubber dam will be applied and tooth will be disinfected as before. The previously sampled canal will be re-entered, flushing with saline and a second periapical sample (S4) will be taken. After the sampling, final flush with 2.5% NaOCL and 17% Ethylene diamine tetraacetic acid (EDTA) in the control group, and with 2.5% NaOCL and 9% Etidronate in the intervention group. Master cones of (0.40) taper gutta-percha will be fitted to the working length and a radiograph will be taken to ensure proper length. Obturation using resin-based root canal sealer. The access cavity will be restored with composite resin and occlusal contact will be checked.
The patients will be asked to record their pain level on VAS & NRS at 6, 12, 24 and 48 hours .
The details of the endodontic procedure for each patient will be recorded in the patient's procedure chart
Finally, the patient will be appointed after 48 hours to collect the outcome data.

Enrollment

34 estimated patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Patients who are free from any physical or mental handicapping condition with no underlying systemic disease.
Mandibular permanent premolar teeth:
- Diagnosed clinically with pulp necrosis.
- Absence of spontaneous pain
- Slight widening in the periodontal membrane space or with a periapical radiolucency
Patients' acceptance to participate in the trial.
Patients who can understand pain scale and can sign the informed consent

Exclusion criteria

Medically compromised patients: Pain levels and healing following treatment would be compromised as these patients have shown higher incidence of pain and lower healing rate.
Pregnant women: Avoid radiation exposure, anesthesia, and medication.
If analgesics or antibiotics have been administrated by the patient during the past 24 hours preoperatively might alter their pain perception.
Patients reporting bruxism or clenching: Avoid further pressure on an already inflamed tooth inducing subsequent irritation and inflammation.
Teeth that shows association with acute periapical abscess and swelling:

Need special treatment steps which could involve additional visits with incision and drainage. Also, it could influence initiation and progression of postoperative pain.

Greater than grade I mobility or pocket depth greater than 5 mm. Need special surgical and/or periodontal therapy.
Hopeless tooth.
Vital teeth.
Immature teeth.
Radiographic evidence of external or internal root resorption vertical root fracture, perforation, calcification.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

34 participants in 2 patient groups

etidronate in sodium hypochlorite

Experimental group

Description:

It comes in a capsule containing 0.9 g of etidronate powder, which should be mixed immediately with 10 mL of a NaOCl solution of choice directly before treatment, resulting in a combined irrigant containing both active chlorine and approximately 9% etidronate. Irrigation with a total volume of 25 ml for each case

Treatment:

Combination Product: etidronate in sodium hypochlorite

sodium hypochlorite

Active Comparator group

Description:

irrigation with 2.5% NaOCl with a total volume of 25 ml for each case

Treatment:

Combination Product: sodium hypochlorite