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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03728517
Other study ID # 1805708779
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date August 23, 2018
Est. completion date January 1, 2019

Study information

Verified date April 2019
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Managing pain in postoperative patients presents challenges in striking a balance between achieving adequate pain control and over-prescribing opioids that have the potential to contribute to the opioid epidemic. There are no clear guidelines informing postoperative opioid prescribing in obstetrics and gynecology.

The primary aim for this study are to better understand the factors that impact opioid use for pain management in gynecologic surgery patient after discharge. The second aim is to develop a model that incorporates individual patient baseline measures (e.g. anxiety, fibromyalgia score, inpatient narcotic consumption) to predict the amount of opioids needed following discharge.


Description:

Managing pain in postoperative patients presents challenges in striking a balance between achieving adequate pain control and over-prescribing opioids that have the potential to contribute to the opioid epidemic. There are no clear guidelines informing postoperative opioid prescribing in obstetrics and gynecology. A recent study by As-Sanie et al. demonstrated that gynecologists at a large academic medical center prescribe twice the amount of opioids than the average patient uses after hysterectomy.1 Similarly, a study completed at Vanderbilt University Medical Center showed that obstetricians were overprescribing narcotics to patients after cesarean deliveries.2

In addition to rates of opioid prescribing, other factors affect postoperative opioid consumption, including individual patient measures of anxiety, depression, and self-reported pain scores prior to surgery. Preoperative Fibromyalgia symptom scores, STAIT state anxiety scores and NRS pain expectations are independent predictors for morphine consumption following hysterectomy.

There is a pressing need to better understand the factors that impact opioid use in women who undergo gynecologic surgery in order to mitigate the over-use of opioids for pain control upon discharge from the hospital.

Aims:

1. Understand the factors that impact opioid use for pain management in gynecologic surgery patients after discharge.

1. Is opioid consumption during the immediate postoperative recovery phase associated with consumption after discharge?

2. Are variables that are known to be associated with opioid consumption, also associated with opioid consumption after discharge?

3. Are there factors which we can use to predict opioid consumption in postoperative patients?

2. Develop a model that incorporates individual patient baseline measures (e.g. anxiety, fibromyalgia score, inpatient narcotic consumption) to predict the amount of opioids needed following discharge.


Recruitment information / eligibility

Status Terminated
Enrollment 4
Est. completion date January 1, 2019
Est. primary completion date January 1, 2019
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years old or older

- Undergoing vaginal, laparoscopic or robotic gynecologic surgery requiring observation or inpatient stay overnight

- Agree to receiving contact from research staff for follow up

- Can provide two telephone numbers or a telephone number and email address

Exclusion Criteria:

- Unable to provide informed consent

- Age <18

- Intolerance/allergy to more than two narcotic medications

- Allergy/contraindication to non-steroidal anti-inflammatory drugs (NSAIDs)

- Has a diagnosed gynecologic malignancy other than Grade 1 endometrial cancer

- Pregnant

- Current opioid use on a regular basis (more than twice per week)

- Illicit drug-use within the past 30 days

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Eskenazi Health Hospital Indianapolis Indiana
United States Indiana University Indianapolis Indiana
United States Methodist Hospital Indianapolis Indiana

Sponsors (1)

Lead Sponsor Collaborator
Indiana University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Understand the factors that impact opioid use for pain management in gynecologic surgery patients after discharge. Is opioid consumption during the immediate postoperative recovery phase associated with consumption after discharge?
Are variables that are known to be associated with opioid consumption, also associated with opioid consumption after discharge?
Are there factors which we can use to predict opioid consumption in postoperative patients?
1 year
Secondary Develop a model 2. Develop a model that incorporates individual patient baseline measures (e.g. anxiety, fibromyalgia score, inpatient narcotic consumption) to predict the amount of opioids needed following discharge. 1 year
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