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Effect of preoperative nasal administration of dexmedetomidine on postoperative delirium in elderly patients with preoperative anxiety after laparoscopic radical resection of colorectal cancer

Effect of preoperative nasal administration of dexmedetomidine on postoperative delirium in elderly patients with preoperative anxiety after laparoscopic radical resection of colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094295
Enrollment
Unknown
Registered
2024-12-19
Start date
2024-12-23
Completion date
Unknown
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Delirium

Interventions

Dexmedetomidine group:Dexmedetomidine hydrochloride nasal spray (1ml:500ug) was given to patients in DEX group from 20:30 to 21:30 on the day before surgery. One spray was injected into each side of t
Control group:Control group was given equal volume 3 injection of normal saline from 20:30 to 21:30 the day before surgery

Sponsors

The First Affiliated Hospital of Hebei North University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 79 Years

Inclusion criteria

Inclusion criteria: (1) Age 65~79 years old; (2) ASA LEVELS I-III; (3) BMI 11; (6) All patients and their families signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients who are unable to sign the informed consent form; (2) Patients who do not understand Chinese; (3) Severe respiratory disease or cardiovascular disease; (4) Severe liver disease (Childs-Pugh score class C); (5) Severe audio-visual impairment affecting communication; (6) Patients with dementia or the score of the preoperative Mini-mental state examination (MMSE) is lower than the minimum score of the corresponding education level (17 points for illiterate >, 20 points for primary school >, and 24 points > middle school or above); (7) Patients receiving psychotropic medication before surgery; (8) Patients with a history of alcohol consumption who received a score of 15 points on the Alcohol Use Disorders Identification Test (AUDIT) > 15 points; (9) History of previous nasal surgery or diseases affecting nasal administration; (10) Allergy or contraindication to the study drug; (11) Those who could not have postoperative follow-up; (12) Severe bradycardia, second-degree/third-degree atrioventricular block; (13) Patients with severe snoring.

Design outcomes

Primary

MeasureTime frame
Incidence of delirium during recovery from anesthesia;Incidence of delirium ;Operation duration;

Secondary

MeasureTime frame
Ramsay score ;From the time of administration of dexmedetomidine or saline until Ramsay score >=3;HR and MAP;Anesthesia duration;Extubation duration;Duration of stay in PACU;Use of vasoactive drugs;Use of narcotic drugs;Sedation and agitation score during waking period;Pain score 10min after extubation and 12h and 24h after extubation;Anxiety scores 1 day before surgery and at 7:00 on the day of surgery (before surgery);Recovery quality scores of patients ;The level of interleukin-6 in venous blood ;neurofilament light (NfL) levels in venous blood;The level of phosphorylated neurofilament heavy subunit -H in venous blood;The number of consecutive 1-minute episodes of hypotension/hypertension during the operation;Incidence of postoperative nausea and vomiting;Incidence of postoperative dizziness;The number of intraoperative bradycardia (heart rate < 50 beats /min);Anesthesia recovery time;

Countries

China

Contacts

Public ContactYao Jie; Zhang Yuxi

The First Affiliated Hospital of Hebei North University

jingjie1229@163.com+86 155 3039 0226

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026