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Effect of dexmedetomidine nasal spray on gastrointestinal function recovery after laparoscopic pediatric hernia surgery

Effect of dexmedetomidine nasal spray on gastrointestinal function recovery after laparoscopic pediatric hernia surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088326
Enrollment
Unknown
Registered
2024-08-15
Start date
2024-08-15
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Postoperative gastrointestinal dysfunction

Interventions

Dexmedetomidine group (DEX group):30 minutes before surgery, intranasal dexmedetomidine is administered in the waiting area. Children with a body weight between 10.7 kg and 19.4 kg receive 30 µg of de
Normal saline group (NS group):Two sprays of saline (one spray in each nostril) are administered in the waiting area 30 minutes before surgery.

Sponsors

Lianyungang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1: Pediatric patients undergoing elective laparoscopic hernia repair; 2: Children aged 2-6 years; 3: American Society of Anesthesiologists (ASA) grade I-II; 4: Parents of the pediatric patients have acceptable proficiency in reading, writing, and speaking Chinese; 5: Both the pediatric patients and their parents voluntarily participate in this study and sign the relevant informed consent forms.

Exclusion criteria

Exclusion criteria: 1: Patients with a history of oral sedative and analgesic medication (benzodiazepines, barbiturates, NSAIDs, opioids, etc.) within 14 days preoperatively; 2: Patients diagnosed with cognitive, consciousness, or developmental disorders; 3: Patients diagnosed with gastrointestinal dysfunction; 4: Patients with contraindications to or allergic reactions to dexmedetomidine; 5: Patients with severe sinus bradycardia or atrioventricular block; 6: Patients with severe nasal diseases; 7: Patients with a history of previous surgeries; 8: Patients with a BMI greater than 25 kg/m².

Design outcomes

Primary

MeasureTime frame
Time to first flatus;Postoperative behavioral changes;

Secondary

MeasureTime frame
Time to first defecation;in-take, feeling nauseated, emesis, exam, and duration of symptoms scoring system,I-FEED;mYPAS-SF scores of children;Parental STAI scores;UMSS score;Parent-child separation score;Postoperative pain;

Countries

China

Contacts

Public ContactFeng Jiying

Lianyungang First People's Hospital

fengjysd@163.com+86 189 6132 2506

Outcome results

None listed

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