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NCT Number: NCT07746323

Effect of Modified Arm Positioning on Shoulder Pain After Thoracoscopic Lobectomy

This study is a prospective randomized controlled trial aiming to reduce shoulder pain after lung surgery. Shoulder pain on the surgical side is common after video-assisted thoracoscopic lobectomy, affecting about 20%-58% of patients. It can limit coughing, moving, and sleeping, and may delay recovery.

The pain may come from two sources: nerve stimulation during surgery and the prolonged arm position used during the operation. While nerve stimulation is hard to avoid, the arm position can be modified. Currently, most pain treatments rely on medications or nerve blocks given after surgery, which have side effects or risks. No one has tried to prevent the pain by changing the arm position during the operation.

We plan to enroll 270 patients scheduled for thoracoscopic lung removal surgery at Chengdu Shangjin Nanfu Hospital. Patients will be randomly divided into two groups. One group will receive the standard side-lying position with arms extended on arm boards (traditional position). The other group will receive a modified position where both arms are bent at the elbows and wrapped with surgical drapes, without using arm boards (modified double-arm wrap position).

Our main goal is to compare the rate of shoulder pain (on the operated side) within 24 hours after surgery between the two groups. We will also compare pain on the opposite shoulder, pain severity, time needed to set up the position, total surgery time, hospital stay, and any nerve or skin complications.

This study has been approved by the Biomedical Ethics Review Committee of West China Hospital, Sichuan University. All participants will provide written informed consent. The findings may help improve intraoperative positioning and enhance early recovery after lung surgery.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chengdu Shangjin Nanfu Hospita

Chengdu, Sichuan, 610011, China

Location status: Recruiting

Location contact

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥18 years.
  • Diagnosed with pulmonary space-occupying lesion and scheduled for elective video-assisted thoracoscopic standard lobectomy.
  • ASA physical status classification I-III.
  • No pre-existing shoulder pain or shoulder mobility impairment prior to surgery.
  • No long-term use of analgesic medications (>1 week) before surgery.
  • Willing and able to provide written informed consent.

Exclusion criteria

  • Severe cervical spine disease or history of brachial plexus injury.
  • Cognitive impairment or psychiatric disorder precluding understanding of pain assessment scales.

Treatment and study plan

Modified Double-Arm Wrap Positioning

Other

Participants in this arm are placed in the standard lateral decubitus position with a thin pillow under the lower side. Both upper arms are abducted to slightly less than 90 degrees, with elbows flexed at 90 degrees. A soft pad is placed between the hands. The forearms are positioned forward above the head, and both arms are wrapped together with surgical drapes for secure fixation. No arm boards are used. This modified position is maintained throughout the entire surgical procedure.

Traditional Arm-Board Position

Other

Participants in this arm are placed in the standard lateral decubitus position with a thin pillow under the lower side. The contralateral upper arm is abducted to slightly less than 90 degrees with the elbow extended, and the forearm is placed on an arm board with a strap secured at the elbow. The ipsilateral arm is similarly positioned on a separate arm board. Both arm boards are used for fixation throughout the entire surgical procedure.

Primary outcomes

  1. Incidence of Ipsilateral Shoulder Pain Within 24 Hours Postoperatively

    Time frame: Within the first 24 hours after surgery

Secondary outcomes

  1. Incidence of Contralateral Shoulder Pain Within 24 Hours Postoperatively

    Time frame: Within the first 24 hours after surgery (Postoperative Day 1, 0-24 hours)

  2. VAS scores for Ipsilateral Shoulder Pain at rest and on movement at 24 h postoperatively.

    Time frame: At 24 hours postoperatively

  3. incidence of ipsilateral shoulder pain at postoperative day 3

    Time frame: Postoperative Day 3

  4. Positioning Setup Time

    Time frame: Intraoperative recording

  5. Total Surgical Duration

    Time frame: Intraoperative recording

  6. Postoperative Hospital Stay

    Time frame: At hospital discharge

  7. Incidence of Brachial Plexus Injury-Related Signs Within 72 Hours Postoperatively

    Time frame: Within 72 hours postoperatively

  8. Position-related pressure injury within 72 h

    Time frame: From the end of surgery to 72 hours postoperatively

Study contacts

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

Sponsors and collaborators

Lead sponsor

Chengdu Jinjiang Maternity and Child Health Hospital

Other

Registry information

Official study title

Effect of Modified Bilateral Arm Wrapping Position on Postoperative Ipsilateral Shoulder Pain in Patients Undergoing Video-Assisted Thoracoscopic Lobectomy: A Prospective Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Aug 5, 2026
Registry last updated
Aug 5, 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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