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Clinical Trials/CTRI/2021/05/033365
CTRI/2021/05/033365
Not yet recruiting
未知

Effect of various cryotherapy applications on postoperative oral health related quality of life in symptomatic irreversible pulpitis- A randomized clinical trial

Dr veluru jyothshna0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: K040- Pulpitis
Sponsor
Dr veluru jyothshna
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Dr veluru jyothshna

Eligibility Criteria

Inclusion Criteria

  • 1\.Patients with symptomatic irreversible pulpitis with apical periodontitis.
  • 2\.Patients of age group between 18\-50 yrs.
  • 3\.Patients who will show prolonged response even after the removal of the stimulus.
  • 4\.Patients will be included in the study after evaluation of electric pulp testing response.
  • 5\.Patient who has the ability to understand the use of OHIP\-14 and pain questionnaires will be provided informed consent for endodontic treatment

Exclusion Criteria

  • 1\.Patients with immature teeth, sinus tract, periapical abscess or facial cellulitis.
  • 2\.Patients with generalised attrition.
  • 3\.Patients with Re \-RCT will be excluded.
  • 4\.Patient with known allergies, or any contra\-indication to opioid or non\-opioid analgesics including aspirin or NSAIDs.
  • 5\.Patients with known allergy to local anaesthesia, sodium hypochlorite and chlorhexidine.
  • 6\.Presence of systemic diseases like cardiovascular disease, renal disease, bleeding disorders or any anti\-coagulant use with in last month.
  • 7\.Pregnant and lactating mothers.
  • 8\.Patients under pain medication for dental or any other illness within 24 hours.
  • 9\.Patients who are unable or unwilling to complete the OHIP\-14 and pain questionnaires.
  • 10\.Patients who are unwilling to sign consent for endodontic treatment.

Outcomes

Primary Outcomes

Not specified

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