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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03933930
Other study ID # N201803039
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date May 6, 2019
Est. completion date May 15, 2021

Study information

Verified date May 2020
Source Taipei Medical University WanFang Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hyperthermic intraperitoneal chemotherapy is a major surgery for tumor peritoneal metastasis. For anesthesiologist, the intra-operative fluid control is always a big challenge. We try to compare the prognosis of lactate-directed and goal-directed therapy. We expect to confirm the better prognosis of lactate-directed therapy.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 15, 2021
Est. primary completion date May 15, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients receiving hyperthermic intraperitoneal chemotherapy

Exclusion Criteria:

- Unable to set arterial line Severe liver or renal disease Severe heart disease Unconscious patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Lactate-directed therapy
If the lactate level elevates, we transfuse pRBC to increase Hct>30%. If Hct >30%, dopamine infusion starts.
Goal-directed therapy
If SVV>15%, transfuse lactate ringer/normal saline alternatively to keep SVV<15%.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary pulmonary complication X-ray findings of airspace or interstitial opacity, lobar consolidation, or pleural effusions; severe respiratory failure requiring respiratory support 1 week
Secondary Renal complication oliguria with urine output<0.5 ml/kg/h for more than 4 h, creatinine increase>30 % of preoperative values, dialysis 1 week
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