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Mobile drainage with high suction versus mobile drainage with low suction.

The influence of suction on chest drain duration and fluid output after lobectomy using only electronic chest drainage systems – a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10408356
Enrollment
100
Registered
2018-04-13
Start date
2015-03-03
Completion date
Unknown
Last updated
2020-01-21

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

Conditions

Pulmonary lobectomy Surgery Pulmonary lobectomy

Interventions

Following pulmonary lobectomy (lower or upper lobes) patients are randomly assigned (1:1) by sequentially numbered, opaque, and sealed envelopes to one of two groups. Participants receive either low e
patients have to be well pain managed and mobilized. There is no upper limit on fluid output (providing it is serous and no chylous). Air leak is < 20 ml/min with no spikes for 6 hours or < 50 ml/min

Sponsors

Department of Cardiothoracic and Vascular Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Admitted for lobectomy (by thoracotomy or video-assisted thoracoscopic surgery [VATS] as decided by the surgeon) 2. Aged over 18 years 3. Ability to give informed consent

Exclusion criteria

Exclusion criteria: 1. Previous history of pulmonary or cardiac surgery 2. Expected difficulties with postoperative mobilization 3. Participation in concomitant research studies in our department in which a different chest drainage protocol could influence these results 4. Anticipation of a need for postoperative mechanical ventilation 5. Insertion of more than one chest drain 6. Bilobectomy or middle lobectomy

Design outcomes

Primary

MeasureTime frame
Duration of air leakage is measured using the time of end of surgery and the time when the chest drain was removed (information from electronic patient charts).

Secondary

MeasureTime frame
1. Fluid output is measured by recording measurements from the drainage device cannister on the patient chart. 2. Length of stay is recorded from hospital records. 3. Re-insertion of chest drains (complications) is recorded using the information from the patient chart.

Countries

Denmark

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 4, 2026