Use of Pain Medication Following Periodontal Procedures

Pain Clinical Trial

Official title:

Anticipated Versus Actual Pain Associated With Periodontal Surgery and Use of Pain Medication

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03064178
• Other study ID #: 13-172
• Status: Completed
• Phase: N/A
• First received: February 19, 2017
• Last updated: February 21, 2017
• Start date: May 10, 2014
• Est. completion date: August 15, 2016

Study information

• Verified date: February 2017
• Source: Brock University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study had the following aims: i. to determine the relationship between anticipated pain and actual pain experienced following periodontal surgery; and ii. determine the factors that predict the amount of pain and the amount of pain medication use following periodontal surgery.

It was hypothesized that experienced pain will be significantly less than anticipated pain. It was also hypothesized that the following factors will affect pain experienced: sex, type of surgery, nervousness, anticipated pain, sedation, age, smoking status, supplement use and pain pill usage. It was hypothesized that the following factors will affect pain pill usage: sex, type of surgery, nervousness, anticipated pain, sedation, age, smoking status, supplement use, and actual pain.

Description:

Patients may delay or avoid periodontal procedures because of fear of dental pain they will experience. By understanding factors that influence pain experienced, practitioners can provide potentially provide accommodations for their patients. This study investigated if anticipated pain is similar to actual pain experienced and if there are certain factors that influence the amount of pain experienced and/or pain pill usage.

Patients kept a 7 day diary in which they recorded anticipated pain (prior to periodontal surgery) and actual pain experienced for 7 days following the surgical procedure. Patients recorded their pain (anticipated and actual) using a visual analog scale (VAS). Patients also recorded daily pain medication and nutritional supplement use in the 7 day diary.

Other information recorded included factors that could influence pain experienced and pain pill use. For pain experienced, the influence of the following factors were assessed: sex, age, type of surgery, nervousness, sedation use, smoking status, anticipated pain, nutritional supplement use and pain pill use. For pain pill use, the influence of the following factors were assessed: sex, age, type of surgery, nervousness, sedation use, smoking status, anticipated pain, nutritional supplement use and pain experienced. These factors were analyzed using regression analyses.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 213
• Est. completion date: August 15, 2016
• Est. primary completion date: March 7, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

• require dental implant surgery or soft tissue graft surgery

Exclusion Criteria:

• regularly took pain medication for pre-existing health conditions

• previous implant or soft tissue graft surgery

Related Conditions & MeSH terms

• Gingival Diseases
• Pain
• Periodontal Diseases

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Brock University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Relationship between anticipated pain and actual pain experienced	Visual analog scale used (mm)	7 days