Oral Caffeine Use for Pain Management in AIS Patients After Spinal Fusion

Study Purpose

Prospective, randomized control trial To determine if oral caffeine decreases the frequency of opioid demand in children with adolescent idiopathic scoliosis after their spinal fusion surgery To compare pain scale ratings, number of requests for diazepam, average heart rate, average blood pressure, sex, age, ethnicity, post-op day of discharge, operative time, estimated intraoperative blood loss, remittance post-surgery, length of hospital stay, and segments fused during spinal fusion surgery.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 12 Years - 17 Years
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - must meet criteria for surgical correction of scoliosis.
  • - must be able to swallow pills.
  • - must have English as a primary language.
  • - must possess mental capacity to understand purpose of the study.
  • - patient must carry diagnosis of adolescent idiopathic scoliosis.
  • - surgery must be performed via posterior approach.
  • - operation performed by either Dr.
John T. Anderson, Dr. Richard M. Schwend, Dr. Aaron Shaw, Dr. Michael Benvenuti.
  • - post-surgical AIS patients from June 2019-June 2024.
  • - the patient must be between the ages of 12 and 17 years old.
  • - the patient and one of their biological parents or guardian(s) must give consent for patient to be included in this study.
  • - Negative Suicide screen.

Exclusion Criteria:

  • - obesity, as defined by a BMI at or above the 95th percentile.
  • - weight below 40 kg.
  • - any orthopedic diagnosis other than AIS.
  • - revision spine surgery.
  • - anterior or combined approach.
  • - admission to PICU post-op.
  • - use of Oxycodone post-op.
  • - allergies to ibuprofen, caffeine, codeine, or diazepam.
  • - history of renal disease.
  • - history of a coagulation disorder.
  • - history of cardiac dysrhythmia or open heart surgery.
  • - history of Chronic Pain Syndrome or Complex Regional Pain Syndrome.
  • - current use of oral central nervous system stimulant (e.g. methylphenidate) - Positive Suicide screen.
The following populations will be excluded:
  • - Children over the age of 18, or turning 18 during time of surgical treatment.
  • - Children or parents unable to consent.
  • - Individuals with cognitive delays.
  • - Pregnant females.
  • - Prisoners.
- Wards of the state

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT04950660
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

Phase 4
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Children's Mercy Hospital Kansas City
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Anne S Stuedemann, APN, MSN
Principal Investigator Affiliation CHILDREN'S MERCY HOSPITALS & CLINICS
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Adolescent Idiopathic Scoliosis
Additional Details

Because these receptors are so important for modifying pain and inflammation, caffeine has been added as an adjuvant to common analgesics, such as paracetamol, ibuprofen, and aspirin in the belief that it will enhance their analgesic efficacy. Most studies used paracetamol or ibuprofen with 100 mg to 130 mg caffeine, and the most common pain conditions studied were postoperative dental pain, postpartum pain, and headache. There was a small but statistically significant benefit with caffeine used at doses of 100 mg or more, which was not dependent on the pain condition or type of analgesic. Additionally, trials have shown superior efficacy of adding caffeine to ibuprofen instead of administering ibuprofen alone for treating acute pain, reflecting that caffeine is an effective analgesic adjuvant. The addition of caffeine (≥ 100 mg) to a standard dose of commonly used analgesics provides a small but important increase in the proportion of participants who experience a good level of pain relief. Finally, the beneficial effects of caffeine on aerobic activity and resistance training performance are well documented. Studies have shown that caffeine ingestion resulted in significantly lower levels of soreness compared with placebo (p ≤ 0.05). A further beneficial effect of sustained caffeine ingestion in the days after the exercise bout is an attenuation of delayed onset muscle soreness. Orthopaedic surgery also causes muscle injury, and patients might benefit from caffeine's effect on lowering muscle soreness. Acute caffeine administration also has been shown to demonstrate increases in alertness, contentment, motivation to work, talkativeness, and energy. It also decreases muscle twitches. All of these effects would be beneficial in the post-operative period, especially for Adolescence Idiopathic Scoliosis (AIS) patients undergoing spinal fusion surgery in the orthopaedic department at Children's Mercy Hospital.

Arms & Interventions

Arms

Active Comparator: Caffeine arm

Experimental Group: patient group (n = 34) receiving a 100 mg dose of caffeine (1/2 of a 200mg tablet to be taken whole or crushed), taken twice daily. This will be an adjuvant to their standard pain control.

Placebo Comparator: Placebo arm

Control group: patient group (n = 34) receiving placebo compounded to look similar to the caffeine treatment, taken twice daily. This will be an adjuvant to their standard pain control.

Interventions

Drug: - Caffeine Tablet

Caffeine is approved by the FDA as a stimulant. A stimulant approved by the United States Food and Drug Administration (FDA) for the treatment to increase mental alertness and in combination with painkiller to treat migraine headaches. It is approved in the form of pill or tablet.

Drug: - Placebo

Placebo, empty opaque dark blue blank capsule, taken twice daily. This will be an adjuvant to their standard pain control.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Children'S Mercy Hospitals & Clinic, Kansas City, Missouri

Status

Recruiting

Address

Children'S Mercy Hospitals & Clinic

Kansas City, Missouri, 64114

Site Contact

ANNE STUEDEMANN, APN, MSN

[email protected]

816-234-3693