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DEGREE OF PERFUSION AS A PREDICTOR FOR FALL IN BLOOD PRESSURE IN ELDERLY PATIENTS UNDERGOING HERNIA SURGERY UNDER SPINAL ANAESTHESIA

PERFUSION INDEX AS A PREDICTOR FOR HYPOTENSION IN ELDERLY PATIENTS UNDERGOING HERNIOPLASTY UNDER SPINAL ANAESTHESIA-AN OBSERVATIONAL STUDY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/01/061751
Enrollment
40
Registered
2024-01-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

CALCUTTA NATIONAL MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA PHYSICAL STATUS I AND II UNDERGOING ELECTIVE HERNIOPLASTY UNDER SPINAL ANAESTHESIA

Exclusion criteria

Exclusion criteria: 1) PATIENTS HAVING CONTRAINDICATIONS FOR SPINAL ANAESTHESIA,LIKE LACK OF CONSENT, RAISED INTRACRANIAL TENSION,INFECTION AT LOCAL SITE, SEVERE AORTIC STENOSIS, COAGULOPATHY,CARDIOVASCULAR INSTABILITY 2) PATIENTS WITH KNOWN ALLERGY TO THE DRUGS INJECTION HEAVY BUPIVACAINR AND FENTANYL 3)PATIENTS RECEIVING ANTIHYPERTENSIVE MEDICATIONS OR VASODILATOR AGENTS 4) PATIENTS WITH BMI >30kg/m2 5)PATIENTS HAVING HEIGHT 6)PATIENTS ASA PHYSICAL STATUS III OR MORE 7) PATIENTS HAVING MAJOR CARDIOVASCULAR,RESPIRATORY,RENAL,HEPATIC ,NEUROLOGICAL OR ENDOCRINE DISEASES 8)PATIENTS REQUIRING GENERAL ANAESTHESIA

Design outcomes

Primary

MeasureTime frame
CORRELATION BETWEEN BASELINE PERFUSION INDEX AND THE CHANGES IN MEAN ARTERIAL PRESSURE IN THE INTRAOPERATIVE PERIODTimepoint: 12 months

Secondary

MeasureTime frame
1) CORRELATION BETWEEN BASELINE PERFUSION INDEX AND THE CHANGES IN SYSTOLIC BLOOD PRESSURE AND DIASTOLIC BLOOD PRESSURE INTRAOPERATIVELY 2) CORRELATION BETWEEN BASELINE PERFUSION INDEX AND TIME OF REQUIREMENT OF FIRST DOSE OF PHENYLEPHRINE,TOTAL PHENYL EPHRINE REQUIREMENT , TOTAL INTRAVENOUS FLUID REQUIREMENT AND INCIDENCE OF NAUSEA AND VOMITINGTimepoint: 12 months

Countries

India

Contacts

Public ContactSREELAKSHMI PV

CALCUTTA NATIONAL MEDICAL COLLEGE AND HOSPITAL

sudeshna04cmc@yahoo.co.in8777725424

Outcome results

None listed

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