Patient Control Epidural Versus Conventional Epidural.

Liaquat National Hospital & Medical College

Status: Invitation-only

Conditions: Length of Hospital Stay; Amount of Analgesic Used; Degree of Motor Block; Sedation Score; Post Operative Pain, Acute

Study type: Observational

Funder types: Other

Identifiers

NCT06721000

App # 0881- 2023- LNH - ERC

Details and patient eligibility

About

As one of the complications of THR is post operative pain, which usually requires epidural catheter insertion.

We are comparing the effect of patient control epidural versus conventional epidural for patient's satisfaction.

Full description

More than 20 years of successful usage of epidural analgesia for post operative pain treatment include intermittent provider-administer bolus, patient control analgesia and continuous epidural infusion with or without patient control epidural analgesia. The main drawback of conventional epidural infusion is that it does not allow for individual variation in management of pain. As a result, patient control epidural analgesia has replaced it in recent years.3. It has been demonstrated that continuous epidural infusion with patient control epidural analgesia is highly effective at providing consistent analgesia, improving patient satisfaction, and reducing the workload of anesthesia provider but it is linked to higher local anesthetic consumption4 In patient undergoing THR, patient control epidural analgesia may be considered as an appropriate alternative for managing post operative pain.

Enrollment: 60 estimated patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Age >18 years. ASA 1-2 on pre anesthesia evaluation. Spontaneous breathing. Spo2 >95% Informed consent for participation.

Exclusion criteria

A history of long-term opioid therapy (use of opioid analgesic at doses higher than codeine 120mg/day, hydrocodone 40mg/day, tramadol 200mg/day or oxycodone 40mg/day 0-4 days before surgery).

Indication of revision surgery during immediate post operative care. Acute skin disease. Patients' refusal. ASA 3 and 4. Hypersensitivity to study drugs.

Trial design

60 participants in 2 patient groups

PCEA group

Description:

Epidural catheter is inserted and patient is given a remote to control the amount of drug given through patient control epidural pump.

Non-PCEA group

Description:

Epidural catheter is inserted and the amount of drug set will be delivered via infusion pump.