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NCT Number: NCT07441785

Immediate and Functional Results of Different Types of Reconstructions After Proximal Gastrectomy For Gastric and Esophagogastric Junction Cancer

Proximal gastric and esophagogastric junction cancers comprise up to 40% of gastric malignancies. For localized disease, proximal gastrectomy is the main radical procedure, but reconstruction of GI tract often leads to significant functional issues.

Rising use of proximal resections and broader indications have increased attention to postoperative quality of life (QoL). Common reconstructions include direct esophagogastrostomy (various types), double-tract reconstruction, jejunal interposition, and newer anti-reflux anastomoses (e.g., double-flap, overlap, tunnel techniques).

Each method has unique pros and cons regarding reflux esophagitis, food passage, dumping syndrome, nutritional changes, and long-term QoL.

No consensus exists on the optimal technique, leading to variable practices and outcomes. Most research focuses on oncologic radicality and survival, while functional results and QoL remain understudied.

Systematic evaluation of functional outcomes across reconstruction types after proximal subtotal gastrectomy is needed in Russian Federation to improve QoL, advance research, and standardize treatment of proximal gastric and EGJ cancers.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

P.Herzen Moscow Oncological Research Institute

Moscow, Russia

Location status: Recruiting

Location contact

Andrey Ryabov, MD, PhD

CONTACT

Anton Kollontai

SUB_INVESTIGATOR

Ilya Kolobaev, PhD

SUB_INVESTIGATOR

About this study

Proximal gastric and esophagogastric junction cancer account for up to 40% of all gastric malignancies. For localized disease, proximal gastrectomy remains the primary radical surgical procedure. However, roconstruction of gastrointestinal continuity after this procedure is associated with significant functional disturbances.

The increasing frequency of proximal resections and expanding indications have heightened focus on postoperative quality of life (QoL). Currently used reconstruction techniques include direct esophagogastrostomy (in various modifications), double-tract reconstruction, jejunal interposition, and emerging anti-reflux esophagogastric anastomoses (e.g., double-flap technique, single-overlap, tunnel reconstruction, etc).

Each method carries distinct advantages and disadvantages concerning reflux esophagitis, food passage, dumping syndrome, nutritional status alterations, and long-term QoL.

Despite this variety, no universal consensus exists regarding the optimal reconstruction technique, resulting in heterogeneous surgical practices and variable functional outcomes. Most studies prioritize oncologic radicality and overall survival, whereas functional results and QoL remain under-investigated.

To enhance patient QoL, advance research, and standardize treatment of proximal gastric and esophagogastric junction cancers in the Russian Federation, there is a clear need for systematic evaluation of functional outcomes across different reconstruction types following proximal subtotal gastrectomy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All consecutive patients with clinically documented primary Gastric or Esophagogastric Junction malignancy (including Siewert I and II) cT1-3N0-2M0 undergoing proximal gastrectomy with curative intent - via open, laparoscopic or robotic approach between 01th January 2025 and 31th December 2026

Exclusion criteria

  • Patients with clinical evidence of metastatic disease, including positive peritoneal cytology on a previous staging laparoscopy, or those with known synchronous other cancers.
  • Esophagogastric Junction Siewert I malignancy
  • Patients submitted to Emergency surgery or surgery without curative intent
  • Patients undergoing any other surgery in addition to the curative surgery for primary Esophageal or Esophagogastric Junction malignancy
  • Patients who have previously undergone surgery on the stomach or colon

Treatment and study plan

proximal gastrectomy

Procedure

Resection of the upper third to one-half of the stomach and the distal portion of the esophagus with different types of digestive system reconstruction

Primary outcomes

  1. The structure and frequency of postoperative complications depending on the method of reconstruction, as well as neoadjuvant treatment

    Time frame: within 90 days after operation

    the types of complication is classified into as follows: esophageal anastomotic leak requiring surgical treatment, esophageal anastomotic leak not requiring surgical treatment, gastric stump necrosis, postoperative bleeding requiring surgical treatment, postoperative bleeding not requiring surgical treatment, postoperative ileum, postoperative pancreatic fistula type B, postoperative pancreatic fistula type C, duodenal stump leak / duodenal stump insufficiency, impaired evacuation from the gastric stump (more than 10 days after surgery), postoperative intestinal perforation or necrosis, persistent air leak through the pleural drain, wound dehiscence (evisceration, hernia), incarcerated diaphragmatic hernia, chylothorax or other types of lymph leakage, infectious complications of the postoperative wound, other complications requiring repeat intervention or another invasive procedure, other.

  2. Overall survival

    Time frame: 1 year after operation

    Overall survival within 1 year after operation

  3. Frequency of local recurrence

    Time frame: 1 year after operation

    Frequency of local recurrence within 1 year after operation

  4. Frequency of tumor progression

    Time frame: 1 year after operation

    Frequency of tumor progression within 1 year after operation

Secondary outcomes

  1. Incidence of development and the severity of reflux esophagitis

    Time frame: 6 and 12 months after surgery

    Incidence of development and the severity (degree of expression) of reflux esophagitis according to the Los Angeles classification in the postoperative period

  2. Incidence of development of esophageal anastomotic stricture

    Time frame: 6 and 12 months after surgery

    Incidence of development of esophageal anastomotic stricture in the postoperative period.

  3. Incidence and severity of dumping syndrome

    Time frame: 6 and 12 months after surgery

    Incidence and severity of dumping syndrome, along with quality of life assessment in the postoperative period according to the KOQUSS-40 questionnaire at 6 and 12 months postoperatively

  4. Pressure of the esophageal anastomosis

    Time frame: 6 and 12 months after surgery

    Pressure of the esophageal anastomosis in the postoperative period according to esophageal manometry

  5. The level of body weight reduction

    Time frame: 6 and 12 months after surgery

    The level of body weight reduction in the postoperative period

  6. The level of hemoglobin

    Time frame: 6 and 12 months after surgery

    The level of hemoglobin in 6 and 12 months after surgery

  7. Food passage rate through the esophagus and the stump of the stomach

    Time frame: 6 and 12 months after surgery

    The rate of passage of food through the esophagus and the stump of the stomach, as well as evacuation from the stump of the stomach into the small intestine based on scintigraphy of the stomach and esophagus after 12 months after surgery

Study contacts

Contact information is provided by the study sponsor or research team.

Andrey Ryabov, MD, PhD

CONTACT

[email protected]

+7 (495) 150-11-22

Sponsors and collaborators

Lead sponsor

P. Herzen Moscow Oncology Research Institute

Other Gov

Collaborators

  • A.Loginov Moscow Clinical Scientific Center

Registry information

Acronym: PROXISTAT

Important dates

Study start
2025
Primary completion
2028
Study completion
2029
First posted
Mar 2, 2026
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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