ClinicalTrials.gg
RecruitingNCT07807696ECTOP-1031Updated Sep 8, 2026

Olive Oil Before Lung Cancer Surgery to Prevent Chylothorax

An interventional study of Extra-Virgin Olive Oil in Lung Cancer and Chylothorax, sponsored by Fudan University. Recruiting at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by Fudan University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Mar 2026, registered Aug 2026).
  • Started Mar 2026; still recruiting 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
1,036
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 15 studies in Lung Neoplasms by Fudan University — 9 open to participants now, 9 under way, 4 of them phase 3. Lung Neoplasms · Fudan University.

Planned enrollment
Largest of 10
1,036 · median 256
Started
2026
with 3 others
No phase
2 of 15
2 open now
Registered
15th of 15
by date

Among the 15 studies in Lung Neoplasms by Fudan University, this one has the largest planned enrollment of the 10 interventional ones, is one of 4 that started in 2026, is one of 2 with no phase, and was the 15th registered.

By phase

15 studies; the count open now beside each. This study's row is marked.

Observational4 · 2 open
Phase 24 · 1 open
Phase 33 · 3 open
No phasethis study2 · 2 open
Other kind1 · 0 open
Phase 2/31 · 1 open

By the year they started

First in 2013; this study’s year is marked. 4 started in 2026.

Size and results

Median enrollment 256 across the 10 interventional studies, 876 across the 5 observational. Of the 3 that completed or were terminated, 0 (0%) have results posted.

Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 15 studies in Lung Neoplasms by Fudan University, or all of them as a file.
02

Study summary

Chylothorax is a rare but serious complication after lung cancer surgery and mediastinal lymph node dissection. This multicenter randomized trial will evaluate whether drinking 40 mL of extra-virgin olive oil 4 hours before surgery can reduce the occurrence of chylothorax after curative lung cancer resection. A total of 1,036 adults with resectable lung cancer will be assigned in a 1:1 ratio to preoperative oral olive oil or standard preoperative fasting without additional olive oil. The primary outcome is the occurrence of chylothorax within 30 days after surgery. Secondary outcomes include repeat surgery, postoperative complications, chest drainage, length of chest tube use, length of hospital stay, and the safety and tolerability of the intervention.

03

Conditions studied

  • Lung Cancer
  • Chylothorax

Keywords

  • Olive Oil
  • Thoracic Duct
  • Postoperative Complications
04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Voluntary participation and willing and able to complete all study procedures.
  • Age 18 to 80 years, inclusive, at .
  • performance status of 0 or 1.
  • Resectable lung cancer.
  • No prior surgery for lung cancer.
  • Treatment-naive and no prior radiotherapy or chemotherapy.
  • Able to take food orally before surgery.

Exclusion criteria

Exclusion Criteria:

  • Allergy to olive oil or any of its components.
  • History of acute or chronic pancreatitis or severe biliary disease.
  • Fat malabsorption syndrome.
  • Prior ipsilateral thoracic surgery or thoracic radiotherapy or chemotherapy.
  • Unable to comply with preoperative dietary instructions.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,036 participants (estimated)

Study arms

  • Experimental
    Preoperative Olive Oil

    Participants drink 40 mL of extra-virgin olive oil 4 hours before surgery and then continue fasting from food and water until surgery.

    Dietary Supplement: Extra-Virgin Olive Oil

  • No intervention
    Standard Preoperative Fasting

    Participants follow each center's standard preoperative fasting regimen: no food for 8 hours and no water for 2 hours before surgery. No additional olive oil is given.

Interventions

  • Dietary supplementExtra-Virgin Olive Oil

    A single 40 mL dose of extra-virgin olive oil is taken orally 4 hours before curative lung cancer surgery. After ingestion, participants continue fasting from food and water until surgery.

06

What researchers measure

Primary outcomes

  1. Incidence of Postoperative Chylothorax

    Percentage of participants diagnosed with postoperative chylothorax. Chylothorax is defined as pleural drainage fluid triglycerides greater than 110 mg/dL (1.2 mmol/L) or a typical milky appearance of pleural drainage after resumption of oral dietary fat.

    Time frame: Within 30 days after surgery

Secondary outcomes

  1. Incidence of Postoperative Complications

    Percentage of participants with one or more surgery-related postoperative complications, including prolonged air leak, atrial fibrillation or other arrhythmia, postoperative bleeding, pulmonary infection, respiratory insufficiency, bronchopleural fistula, pneumothorax or atelectasis, recurrent laryngeal nerve injury, or death.

    Time frame: Within 30 days after surgery

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07807696
Lead sponsor
Fudan University
Responsible party
Haiquan Chen (director of thoracic surgery department, Fudan University) — Principal investigator
First posted
Sep 8, 2026
Start date
Mar 15, 2026
Primary completion
Jun 1, 2027 (estimated)
Completion
Dec 30, 2030 (estimated)
Last update
Sep 8, 2026

Study contacts

Hang Cao, MD
Contact
16301050173@fudan.edu.cn
+86 18717722753

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion