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Pain Management After Transnasal Transsphenoidal Surgery for Pituitary Adenomas

Not Applicable
Conditions
Pituitary Adenoma
Surgery
Pain
Interventions
Registration Number
NCT04611685
Lead Sponsor
Peking Union Medical College Hospital
Brief Summary

We hypothesize that the effects of non-steroidal anti-inflammatory drugs (NSAIDS) for pain relief among patients with pituitary adenomas undergoing transnasal transsphenoidal surgeries are non-inferior to tramadol. We aim to launch a single-center randomized clinical trial to verify this hypothesis.

Detailed Description

Postoperative pain is an important clinical concern and quality-of-care metric, yet it is undertreated in neurosurgical patients. Approximately 40% of inpatients complain of severe pain postoperatively, and only 56% of these patients indicate that their pain is well controlled. In addition, pain is a common cause of delayed discharge and unplanned hospital readmission.

Pituitary adenoma is the second most common benign primary central nervous system tumor, and transnasal transsphenoidal (TTS) has long taken over craniotomy to be the first-line surgical approach for pituitary tumor resection. TTS significantly reduces patient's surgical trauma, shortens the operation time, reduces surgery-related complications, and increases total tumor resection rate compared with the previously used craniotomy. However, given that the nasal mucosa is extremely sensitive, the feeling of pain is more obvious after surgery via TTS approach than via craniotomy.

Opioids such as morphine and pethidine are the most effective post-surgical analgesics, but they have a series of side effects, such as drug addiction, decreased gastrointestinal motility, nausea and vomiting. Opioids are not an analgesic that must be used after TTS surgery. NSAIDS, such as parecoxib and lexone, and tramadol are also commonly used analgesics after surgery, and they are also effective. NSAIDS is a first-tier painkiller, and tramadol is a second-tier drug. There is no evidence-based evidence recommending the preferred choice of these two drugs. Which of NSAIDS and tramadol has the better analgesic effect and which drug brings lower side effects to patients is still unclear. The clinical application of the two drugs is entirely based on the personal habits of the surgeon.

Therefore, we plan to conduct a prospective randomized controlled trial to explore: whether the analgesic effect of NSAIDS is non-inferior than tramadol; and whether the side effects of NSAIDS are not higher than tramadol. This result will guide us in clinical pain management for patients with pituitary adenomas after surgery via TTS approach.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
202
Inclusion Criteria
  • Patients with pituitary adenomas that need transnasal transsphenoidal surgery
  • Patients of either gender aged 18 to 70 years
Exclusion Criteria
  • Patients with rhinitis, sinusitis, deviated nasal septum, etc. that can cause nasal pain
  • Patients with medical history of digestive ulcer/gastrointestinal bleeding
  • Patients with heart disease, severe liver and kidney dysfunction
  • Pregnant patients
  • Patients allergic to NSAIDs or tramadol
  • Patients who need long-term treatment of NSAIDs or analgesic for other reasons
  • Patients whose postoperative paraffin pathology suggests non-pituitary adenoma
  • Patients who have not undergone transsphenoidal surgery
  • Patients who reject to enter the group or ask to leave the group after entry

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
NSAIDsNSAIDParecoxib (iv.) for once \& Loxoprofen (po.) for routine use during the first 3 postop. days.
TramadolTramadolTramadol (im.) for once \& Tramcontin (po.) for routine use during the first 3 postop. days.
Primary Outcome Measures
NameTimeMethod
The VAS scores of patients24 hours after the surgery

visual analogue scale score that represents the patient's subjective pain perception

Secondary Outcome Measures
NameTimeMethod
The VAS scores of patients72 hours after the surgery

visual analogue scale score that represents the patient's subjective pain perception

The dynamic trend of VAS scores of patients during the first 3 postoperative daysduring the first 3 postoperative days

visual analogue scale score that represents the patient's subjective pain perception

Trial Locations

Locations (1)

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

🇨🇳

Beijing, Beijing, China

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