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Dexmedetomidine Used in Rapid Rehabilitation Strategy for Infants with Congenital Heart Disease

Dexmedetomidine Used in Rapid Rehabilitation Strategy for Infants with Congenital Heart Disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023887
Enrollment
Unknown
Registered
2019-06-15
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

Congenital heart disease

Interventions

Group 3:Paravertebral block combined with dexmedetomidine
Group 4:Dexmedetomidine
Group 5:Postoperative dexmedetomidine was added

Sponsors

Guangzhou Women and Children Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.1 Years to 3 Years

Inclusion criteria

Inclusion criteria: 1) Aged one month to three years, weight 5 kg to 20 kg; 2) ASA I-III; 3) Precocious heart disease surgical risk rating: RACHS level 1-4(RACHS level 3-4 should be cautious); 4) Surgical malformation treatment satisfaction(TEE evaluation anatomy and circulation); 5) Assessment of Breathing Cycle Function at Stop Time: Blood gas: electrolytes; Lung ventilation index ventilation index(carbon dioxide partial pressure, oxygen partial pressure, oxygenation index); P-V ring assessment of lung compliance(especially in preoperative pneumonia); Direct pulmonary arterial pressure measurement(especially in children with preoperative pulmonary hypertension); Circulatory status assessment(application of vasoactive drugs, systolic pressure, mean pressure, pulse pressure difference, EF value, myocardial surface color and myocardial contraction state, pacemaker adjustable arrhythmia, lactic acid value); 6) Extraction time assessment of respiratory circulation function: Breathing(frequency, Tidal volume, oxygen saturation, lung ventilation index); Circulation(application of vascular active drugs, systolic pressure, mean pressure, pulse pressure difference, TEE) Blood gas(acid-base electrolytes, lactic acid); pupil; Urine volume and color.

Exclusion criteria

Exclusion criteria: 1) ASA Level 4-5, RACHS Level 5-6 2) Preoperative treatment for heart failure pneumonia 3) Liver and kidney diseases, with clotting disorders; 4) Poor premature infants 5) Unsatisfactory treatment of surgical deformities Multiple drug support, hemodynamic instability

Design outcomes

Primary

MeasureTime frame
serum cortisol;Insulin;blood glucose;norepinephrine(NE);epinephrine(E);

Secondary

MeasureTime frame
immune factor;Vital signs;Postoperative pain score;Dosage of analgesic drugs;Changes in body temperature;Coagulation function;Inflammatory factor;Operation time;Extracorporeal circulation time;Length of stay;Hospitalization expenses;Tracheal extubation time;

Countries

China

Contacts

Public ContactXingrong Song

Anesthesiology Department, Guangzhou Women and Children Medical Center

447618644@qq.com+86 13922416303

Outcome results

None listed

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