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

Clinical and Biochemical Effects Of Different Cryotherapy Protocols On Endodontic Treated Mandibular Premolars With Symptomatic Apical Periodontitis: A Randomized Clinical Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07138365
Enrollment
180
Registered
2025-08-22
Start date
2024-06-01
Completion date
2025-06-01
Last updated
2026-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain, Inflammation

Keywords

Cryotherapy, post operative pain, inflammation, analgesic intake

Brief summary

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

Detailed description

-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. Cold Irrigation Group : Canals were irrigated with cold (2-4 oC) 2.5% NaOCl. Final flush was done with cold (2-4 oC) Saline for 10 mins. 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. -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.

Interventions

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.

PROCEDUREIntra radicular Cryotherapy

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

PROCEDUREcold irrigation

irrigation with cold (2-4 oC) 2.5% NaOCl and Final flush was done with cold (2-4 oC) Saline for 10 mins.

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

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.

Intervention model description

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Level of inflammatory mediator (substance P) in apical fluidbase line 1st sample:after glide path and coronal flaring for all groups second sample:in control group and intraradicular group taken after mechanical preparation, ,and in oral cryo group after mechanical application and 30 minutes application of cryoSterile 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.After collecting samples from all patients, the samples will be evaluated by the enzyme-linked immunosorbent assay (ELISA) method.

Secondary

MeasureTime frameDescription
level of post operative pain using 10 cm visual analoge scale (VAS)after 6hours, 24hours, 48hours, 72hours h after treatmentOn a10-cm Visual Analogue Scale (VAS) questionnaire, each patient reported their level of pain as follows: There is no pain at 0, 1-3, mild, 4-6, moderate, 7-9, severe, and 10, the worst pain
Analgesic intakeThey will be contacted by telephone at 6, 12, 24, 48 and 72 hours afterThey will be asked if they needed to take the analgesics and the frequency of taking it.

Countries

Egypt

Contacts

STUDY_DIRECTORMaram F Obeid, Professor

Faculty of Dentistry,Ain Shams University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026