UnknownPhase 2ketamine

Esketamine Combined With Pregabalin on CPSP in Spinal Patients.

Sponsored by Beijing Tiantan Hospital

NCT ID
NCT06117917
Target Enrollment
150 participants
Start Date
2023-11-10
Est. Completion
2024-06-30

About This Study

Chronic postsurgical pain has become one of the most common complications of surgery. The quality of life will be impacted once the postsurgical patients are combined with persistent pain. What's more, the postsurgical pain may increase other adverse outcomes. It's important to find a better way to keep the postsurgical patients away from postoperative pain. Esketamine and pregabalin have become potentially effective drugs on CPSP.

Conditions Studied

EsketaminePregabalineChronic Post Operative Pain

Interventions

  • S-ketamine and pregabalin
  • Normal saline and placebo capsule

Eligibility

Age:18 Years - 65 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Patient undergoing elective primary spinal tumor surgery;
* Ages between 18 and 65 years old;
* American Society of Anaesthesiology (ASA) status I-III;
* Signed informed consent.

Exclusion Criteria:

* Previous adverse reaction to ketamine, s-ketamine or pregabalin;
* Patients with a diagnosed history of severe chronic pain;
* Patients with long-term analgesic treatment(gabapentin/opioids/ketamine);
* Patients with aphasia or inability to cooperate with the pain assessments;
* Known sever insufficiency of vitals(such as heart failure/renal dysfunction/hepatic failure);
* Patients with a diagnosed history of psychiatric disorder;
* Patients treated with gabapentin/pregabalin in the last three months;
* Drug abuse;
* Body mass index (BMI) \> 35 kg/m2 ;
* Pregnancy or lactation.

Study Locations (1)

Beijing Tiantan Hospital
Beijing, China

This trial is not recruiting

This study is currently not accepting new participants.

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Data Source
ClinicalTrials.gov

Last updated from source

Esketamine Combined With Pregabalin on CPSP in Spinal Patients. | Huxley