Eye Pain in Post-Operative Ophthalmic Patients in the Recovery Room
Conditions
Interventions
Buccal acupuncture group:Performed by the same experienced anesthesiologist. The buccal needle group received precise insertion of needle bodies containing the needle body at the cervical acupoints, s
Control group:A needle-free medical patch with identical appearance was used, following the same treatment protocol for routine therapy and efficacy observation.
Sponsors
Beijing Tongren Hospital Affiliated to Capital Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: (1)18 to 70 years old; (2)ASAI-III level; (3)Patients who plan to undergo elective ophthalmic surgery under general anesthesia; (4)The NRS score for eye pain after entering the recovery room is >3 points; (5)Agree to this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: (1)Presence of any contraindications to buccal needle therapy (including but not limited to: skin infection or injury in the buccal region; known severe coagulation disorders; significantly reduced platelet count; severe hypersensitivity to buccal needle-related consumables such as adhesive tape or needles); (2)Consciousness impairment or cognitive dysfunction, inability to autonomously express pain or cooperate with the study; (3)Regular use of medications that may affect pain perception or the central nervous system (e.g., opioid analgesics, antidepressants, anticonvulsants) within the past 3 months; (4)The patient or legal representative refuses to sign the informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamic index;Postoperative Nausea and Vomiting;Recovery room stay time;Palliative analgesia;Untoward effect;Satisfaction score; | — |
Countries
China
Contacts
Public ContactGuyan Wang
Beijing Tongren Hospital Affiliated to Capital Medical University
Outcome results
None listed