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Confirmation of Thoracic Epidural Space by the presence of waveform and the depth analysis by ultrasound

Confirmation of Thoracic Epidural Space by Epidural Pressure Waveform Analysis in Adults and Correlation with Ultrasound Guided Epidural Space Depth - A Descriptive Observational Pilot Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/11/010687
Enrollment
40
Registered
2017-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K810- Acute cholecystitis Health Condition 2: null- Adult male and female patients of ASA I OR II with body weight between 45-70 kg and height of 150-180 cm, scheduled for upper abdominal surgeries and thoracic surgeries Health Condition 3: D292- Benign neoplasm of testis Health Condition 4: K800- Calculus of gallbladder with acutecholecystitis Health Condition 5: N200- Calculus of kidney Health Condition 6: K639- Disease of intestine, unspecified Health Condition 7: K650- Ge

Interventions

None listed

Sponsors

university college of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I OR II with body weight between 45-70 kg and height of 150-180 cm, scheduled for upper abdominal surgeries and thoracic surgeries will be included

Exclusion criteria

Exclusion criteria: Non consenting patients, skin infection at the site of injection, history of spinal fractures and coagulation abnormalities, anatomic abnormalities of spinal cord and vertebral bodies, spinal metastasis, hypersensitivity to local anesthetics, raised intracranial tension, raised blood pressure and heart rate and other contraindications to epidural anesthesia.

Design outcomes

Primary

MeasureTime frame
Documentation of epidural waveform through epidural needle and catheter. Timepoint: Immediately after loss of resistance

Secondary

MeasureTime frame
Loss of resistance to saline injection. Sensory dermatomes blocked. Hemodynamic parameters. Timepoint: pre-operative, just before and following the test dose as per test dose protocol and every 5 min after subsequent 7 mL injection of the local anaesthetic solution till 30 min.

Countries

India

Contacts

Public ContactDr Kshitiz Hirani

university college of medical sciences and GTBH

newdraksethi@gmail.com9868399700

Outcome results

None listed

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