Registered outcomes17

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

1 to 17 of 17

List	Outcome	Time frame	Description
Primary	Mechanical pain threshold around the incision at 6 hours post-surgery	6 hours post-surgery	Mechanical pain thresholds around the surgical incision were measured using a von Frey tactile esthesiometer kit.
Secondary	Mechanical pain threshold around the incision	Preoperatively,at 30 minutes post-surgery, at 24 hours post-surgery, at 48 hours post-surgery	Measurements around the incision were taken at the midpoint of the incision and at 5 cm from each end of the incision, and the mean value of all measurement points was calculated.
Secondary	Mechanical pain threshold on the non-dominant forearm	Preoperatively, at 30 minutes post-surgery, at 6 hours post-surgery, at 24 hours post-surgery, at 48 hours post-surgery	Measurements on the non-dominant forearm were taken at 3, 6, and 9 cm from the antecubital crease, and the mean of the three values was calculated.
Secondary	Operative time	Intraoperatively
Secondary	Extubation time	From the end of surgery until tracheal extubation, assessed for up to 2 hours postoperatively	Extubation time, defined as the time from the end of surgery to tracheal extubation
Secondary	PACU stay duration	From PACU admission until PACU discharge, assessed for up to 4 hours after PACU admission	PACU stay duration, defined as the time from PACU admission to PACU discharge
Secondary	Intraoperative propofol consumption	Intraoperatively
Secondary	Intraoperative remifentanil consumption	Intraoperatively
Secondary	Number of patients receiving atropine	Intraoperatively
Secondary	Number of patients receiving vasopressors	Intraoperatively
Secondary	MAP	Preoperatively (baseline), 1 minute after skin closure , at tracheal extubation, immediately before leaving the operating room	Mean arterial pressure (MAP)
Secondary	HR	Preoperatively (baseline), 1 minute after skin closure , at tracheal extubation, immediately before leaving the operating room	heart rate (HR)
Secondary	Numeric Rating Scale (NRS) score	at 30 minutes post-surgery, at 6 hours post-surgery, at 24 hours post-surgery, at 48 hours post-surgery	Numeric Rating Scale (NRS) for pain score ranging from 0 to 10; higher scores indicate worse pain.
Secondary	Number of effective PCA compressions	From end of surgery to 48 hours post-surgery
Secondary	Number of patients requiring rescue analgesia	From end of surgery to 48 hours post-surgery
Secondary	Quality of Recovery-15 (QoR-15)	at 24 hours post-surgery	Quality of Recovery-15 (QoR-15) questionnaire score ranging from 0 to 150 (15 items, each scored 0-10); higher scores indicate better quality of postoperative recovery.
Secondary	Incidence of adverse reactions	From end of surgery to 48 hours post-surgery	ncidence of adverse reactions: The occurrence of adverse events including hypotension, bradycardia, shivering, postoperative nausea and vomiting (PONV), dizziness, drowsiness, respiratory depression, and pruritus within 48 h postoperatively was recorded.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNone stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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