Clinical and Biochemical Effects Of Cryotherapy Protocols On Mandibular Premolars With Symptomatic Apical Periodontitis

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-01

Study Completion Date

2025-06-01

Brief Summary

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Pain is the major reason for patients' visits to dental clinics.Medications have side effects. Treatments including cryotherapy have been suggested to prevent these side effects.This study will compare the effect of oral and intraradicular cryotherapy on the level of substance p ,post operative pain and analgesic intake in mandibular premolars with symptomatic apical periodontitis.

Thirty patients with symptomatic apical periodontitis will be randomly distributed into three groups: oral,intraradicular cryotherapy and control group (n = 10). In the oral cryotherapy group application of (a cold pack of ice gel enveloped by a sealed plastic cover) will be performed for 30 minutes following the completion of canal preparation.Getting glide path by inserting K-file #10. coronal flaring will be done .The first apical fluid samples for all groups will be obtained at this step. Intra-radicular cryotherapy will be performed where normal root canal treatment will be done. Then a final flush will be done with 20 mL of cold saline 2.5°C for 10 minutes.

For the control group,no application of cryotherapy will be done.Second samples will be taken after mechanical preparation for intraradicular and control ,and after 30minutes of cold application for the cryotherapy group.Levels of substance p will be measured using the ELISA test.The patients will be asked to fill out the VAS questionnaire at 6, 24, 48 and 72 h.and analgesic intake

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Detailed Description

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-Oral Cryo Group: All patients will receive anesthesia containing Artinibsa 4%:100,000 epinephrine (Inibsa, Spain) 1.8 mL .

The teeth will be isolated with a rubber dam (Sanctuary) after local anesthesia. Dental caries or restoration of the teeth, if any, will be removed .Access cavity will be done by new tapered stone with round end with copious coolant. Upon pulp exposure, dark profuse bleeding filled the pulp chamber. Initial glide path will be done by inserting K-file #10. After confirming glide path, coronal flaring will be done by orifice opener rotary file (M-Pro 19 taper 8). Working length will be determined by apex locator E PEX (Eighteeth Medical Technology Co., Ltd., Changzhou, China).The working length will be established at 0.5 mm short of the full length as determined by the electronic apex locatorand validated by a periapical radiograph.

First base line apical fluid sample (S1) will be collected at this step. Sterile paper point size 20 taper 2% will be inserted into the canal and placed 2 mm beyond the apex. The paper point will be left for 30 seconds to absorb sufficient amount of fluid. Paper point will be placed into an Eppendorf tube with 1 mL (pH 7.4) phosphate buffered saline and refrigerated at 10°C for later examination.

Mechanical preparation of the canals will be carried out according to the sequence of M pro rotary files kit #20/4, #25/6, #35/4, #40/4. Patency will be checked after each file with #10 k- file. Apical preparation will be further enlarged to manual file #50 or #55 in some cases. During the procedure, irrigation will be performed between each rotary file using a side-vented needle (gauge size 30) positioned 2mm from the working length. This will be done with 5 mL of 2.5% sodium hypochlorite (NaOCl). Followed by 5 ml of 17% EDTA (META BIOMED, Korea) for 1 min.Final flush will be done with room temperature Saline for 10 minutes.

Next, custom made plastic pack measuring 2.5 X5 cm containing ice gel will be placed intraorally in the mouth on the vestibular surface of the treated tooth.

Patients will be instructed to remove the ice pack for 2 minute if they felt extreme cold or a burning sensation. Each pack will be placed for 10 min, totaling three minimally per 30 min of intermittent application with 2-min breaks in between.

During the cryotherapy treatment, a thermocouple device will be used to monitor the temperature, which Will be maintained at 10 °C. If the temperature exceeded the predetermined threshold of 10 °C, immediate replacement of the gel pack with a new one will be carried out to bring the temperature back within the desired range.

After the completion of three cycles, the second sample of AF (S2) will be collected, as described earlier.

-Intra-Radicular Cryo Group: Access cavity was done by new tapered stone with round end with copious coolant. Upon pulp exposure, dark profuse bleeding filled the pulp chamber. Caries and old restoration were removed.

Initial glide path was done by inserting K-file #10. After confirming glide path, coronal flaring was done by orifice opener rotary file (M-Pro 19 taper 8). Working length was determined by apex locator.

First base line apical fluid sample (S1) was collected at this step. Sterile paper point size 20 taper 2% was inserted into the canal and placed 2 mm beyond the apex. The paper point was left for 30 seconds to absorb sufficient amount of fluid.

Mechanical preparation of the canals was carried out according to the sequence of M pro rotary files kit #20/4, #25/6, #35/4, #40/4. Patency was checked after each file with #10 k- file. Apical preparation was further enlarged to manual file #50 or #55 in some cases.

During the procedure, irrigation was performed between each rotary file using a side-vented needle (gauge size 30) positioned 2mm from the working length. This was done with 5 mL of 2.5% sodium hypochlorite (NaOCl), Followed by 5 ml of 17% EDTA (META BIOMED, Korea) for 1 min. Final flush was done with cold (2-4 oC) Saline for 10 mins. Temperature of cold saline was maintained by keeping the irrigation syringes in an ice box filled with cooling gel packs with thermocouple inside to confirm that the temperature within range (2-4 oC). Irrigation syringes were used one by one.

The second sample (S2) was taken after chemo-mechanical preparation and finishing the irrigation protocol.

-Control Group: Patients will receive conventional root canal treatment. Canals will be irrigated with room temperature 2.5% NaOCl. Final flush will be done with room temperature saline for 10 min.First apical fluid sample will be taken after coronal flaring and determining the working length and the second one was taken after chemo-mechanical preparation and finishing the irrigation protocol.

Conditions

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Post Operative Pain Inflammation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

randomized, controlled, single-blinded, single- center clinical trial

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

1)Patients will be assigned at random to either the intra oral group ,intra radicular group or the control group (n=10). The name of the group will be scrawled on a slip of paper and sealed inside a plain envelope. As each patient arrived for treatment, one envelope will be drawn at random from a box to assign the patient to a certain group.

Study Groups

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control group

No application of cryotherapy .Patients will receive conventional root canal treatment. Canals will be irrigated with room temperature 2.5% NaOCl. Final flush will be done with room temperature saline for 10 min.

Group Type NO_INTERVENTION

No interventions assigned to this group

Oral Cryo Group

custom made plastic pack measuring 2.5 X5 cm containing ice gel will be placed intraorally in the mouth on the vestibular surface of the treated tooth.

Patients will be instructed to remove the ice pack for 2 minute if they felt extreme cold or a burning sensation. Each pack will be placed for 10 min, totaling three minimally per 30 min of intermittent application with 2-min breaks in between.

During the cryotherapy treatment, a thermocouple device will be used to monitor the temperature, which Will be maintained at 10 °C. If the temperature exceeded the predetermined threshold of 10 °C, immediate replacement of the gel pack with a new one will be carried out to bring the temperature back within the desired range.

Group Type ACTIVE_COMPARATOR

oral Cryotherapy

Intervention Type PROCEDURE

custom made plastic pack measuring 2.5 X5 cm containing ice gel will be placed intraorally in the mouth on the vestibular surface of the treated tooth.

Intra-Radicular Cryo Group

During the procedure, irrigation was performed between each rotary file using a side-vented needle (gauge size 30) positioned 2mm from the working length. This was done with 5 mL of 2.5% sodium hypochlorite (NaOCl), Followed by 5 ml of 17% EDTA (META BIOMED, Korea) for 1 min. Final flush was done with cold (2-4 oC) Saline for 10 mins.

Group Type ACTIVE_COMPARATOR

Intra radicular Cryotherapy

Intervention Type PROCEDURE

Final flush was done with cold (2-4 oC) Saline for 10 mins.

Interventions

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oral Cryotherapy

custom made plastic pack measuring 2.5 X5 cm containing ice gel will be placed intraorally in the mouth on the vestibular surface of the treated tooth.

Intervention Type PROCEDURE

Intra radicular Cryotherapy

Final flush was done with cold (2-4 oC) Saline for 10 mins.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Both genders
2. Eligible participants will be between the ages of 18-45
3. Participants willing to commit for the entire period of the trial and agreed to sign the written consent after full explanation of the study
4. Having a mandibular single rooted premolar tooth with vital pulp Vertucci Type I canal system.
5. Patients that will be diagnosed with symptomatic apical periodontitis on the basis of the clinical symptoms of severe preoperative pain (visual analogue scale \[VAS\] \> 7) and severe percussion pain (VAS \> 7)
6. The absence of periapical radiolucency on x ray.

Exclusion Criteria

1. Presence of any systemic disease or allergic reactions
2. Vulnerable population: prisoners, pregnant women, mentally ill people, etc.
3. Use of analgesic or antibiotic medication within seven days
4. A radiographically untraceable canal
5. Excessively curved root
6. Excessively long or short root length
7. Teeth with open apices
8. A previous root canal treatment
9. Sinus tracts
10. Local gum swelling around the affected tooth
11. Severe periodontal disease
12. Presence of periodontal pockets \>3 mm in the affected tooth
13. Absence of bleeding in the pulp chamber on access cavity preparation
14. Problems in determining working length
15. Broken files, over instrumentation, and overfilling/incomplete filling

Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes