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Comparing surgically placed jejunal tubes with nasal tubes for feeding in patients undergoing surgery for food pipe cancer.

Comparing feeding jejunostomy with nasojejunal tube placement in patients undergoing oesophagectomy: A pilot study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/05/025445
Enrollment
40
Registered
2020-05-29
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: C159- Malignant neoplasm of esophagus, unspecified

Interventions

Intervention1: Nasojejunal tube: Tube inserted through nose into jejunum intraoperatively. Frequency: 1 tube per patient, randomized to nasojejunal tube placement. Duration of use: Removed 2 days afte

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing oesophagectomy for carcinoma oesophagus.

Exclusion criteria

Exclusion criteria: 1.Those who refuse consent to participate in the study 2.Patients with any nasopharyngeal or oropharyngeal obstruction preventing insertion of nasojejunal tube

Design outcomes

Primary

MeasureTime frame
Rate of complications in both groups of patients: those undergoing nasojejunal tube feeding versus surgical feeding jejunostomyTimepoint: Post operatively, till the time of removal of feeding jejunostomy tube at 6 weeks.

Secondary

MeasureTime frame
1. To compare catheter efficacy of nasojejunal tube feeding with surgical feeding jejunostomy in terms of: Time to full establishment of oral intake Time to removal of feeding tube Timepoint: Postoperatively;2. To compare the discomfort associated with surgical feeding jejunostomy versus nasojejunal tube using the visual analogue scale.Timepoint: From post operative day 2 till the time of removal of nasojejunal tube;3.To compare the quality of life with a surgical feeding jejunostomy with nasojejunal feeding tube using the WHOQOL-BREF questionnaireTimepoint: Self reported at the time of discharge and at 6 weeks follow up.

Countries

India

Contacts

Public ContactDr Lokesh Agarwal

AIIMS, New Delhi

nagranjan@gmail.com9868115535

Outcome results

None listed

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