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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02641938
Other study ID # 3-2015-0262
Secondary ID
Status Completed
Phase Phase 4
First received December 20, 2015
Last updated December 29, 2017
Start date December 2015
Est. completion date November 2017

Study information

Verified date December 2017
Source Gangnam Severance Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate the renal protective effect of dexmedetomidine in patients undergoing cytoreduction and hyperthermic intraperitoneal chemotherapy


Description:

A cytoreductive surgery and hyperthermic intraperitoneal chemotherapy may lead to the renal hypoperfusion, systemic inflammatory response, and oxidative stress. Dexmedetomidine has been known to protect the kidney against inflammation and oxidative stress in diverse clinical settings. It may also enhance a renal perfusion by inhibition of renal sympathoexcitation. We hypothesized administration of dexmedetomidine might protect the kidney in patients undergoing cytoreduction and hyperthermic intraperitoneal chemotherapy.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date November 2017
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of malignant tumor with peritoneal metastasis

- Scheduled for elective cytoreduction and hyperthermic intraperitoneal chemotherapy

Exclusion Criteria:

- Preoperative chronic kidney disease stage =4 defined by KDOQI ( eGFR < 30 mL/min/1.73m2)

- Congestive heart failure

- Atrioventricular block > 1st degree

- Bradycardia < 45 beat per minute

- History of myocardial infarction within 3 months

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dexmedetomidine
Dexmedetomidine group :1ug/kg IV loading over 20 minutes followed by 0.5ug/kg/hr IV infusion after induction of anesthesia until the completion of the surgery
Normal Saline
Control group :IV loading and infusion of same volume of normal saline after induction of anesthesia until the completion of the surgery

Locations

Country Name City State
Korea, Republic of GangnamSH Seoul

Sponsors (1)

Lead Sponsor Collaborator
Gangnam Severance Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Creatinine clearance from baseline Assessment of the creatinine clearance which reflects kidney function during postoperative 7 days Postoperative day 1,2,3,4,5,6,7
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