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Evaluation of text messaging service on management of post-operative pain in opioid-naïve surgical patients

Not Applicable
Conditions
post-operative pain
Anaesthesiology - Pain management
Registration Number
ACTRN12622000516785
Lead Sponsor
Peninsula Health Pharmacy Department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
700
Inclusion Criteria

Inclusion
Adult patients (18 years or older) undergoing surgery requiring at least overnight stay and prescribed opioid medication while in hospital post-surgery AND expected to need opioid analgesia for more than 48 hours after discharge
Surgery Categories and Types
General Surgery
•Inguinal hernia repair
•Laparoscopic cholecystectomy
•Umbilical hernia repair
•Epigastric hernia repair
•AppendectomyBreast surgery
•Simple mastectomy
•Lumpectomy
Colorectal surgery
•Left/sigmoid resection
•Ileocolic resection
•Low anterior resection
•Total colectomyEndocrine neck surgery
•Parathyroidectomy
•Thyroidectomy
Urology
•Laparoscopic prostatectomy
•TURPVascular
•Varicose veins
•Femoral-popliteal bypass
•Toe amputation
Plastic
•Wound debridement
•Skin lesion excisionsGynaecology
•Laparoscopic hysterectomy
•Vaginal hysterectomy
•Total abdominal hysterectomy
•Posterior/anterior repairs
•Laparoscopic oophorectomy

Patients with the ability to consent and the ability to receive and send SMS text messages.

Exclusion Criteria

Exclusion criteria
1.Patients taking opioids at the time of or prior to admission (e.g. on long-term oxycodone, oxycodone/naloxone, morphine, buprenorphine, buprenorphine/naloxone, hydromorphone, methadone, tramadol and tapentadol)
2.Undergone major surgeries with prolonged hospital stays in the past 12 months
3.Patients who have a documented discharge pain plan by the Acute Pain Team
4.Patients who do not understand written and verbal English
5.Patients with substance use disorder history (e.g. alcohol dependence, intravenous drug use) as per hospital medical records.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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